ZFHX4
zinc finger homeobox 4
Summary
Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be located in chromatin. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants289 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs58357751 | 8:77,595,642 | C/T | — | — |
| rs4735738 | 8:77,611,625 | A/T | — | — |
| rs775098927 | 8:77,616,361 | A/G | — | uncertain significance |
| rs2536193807 | 8:77,616,375 | A/C | — | uncertain significance |
| rs777758835 | 8:77,616,387 | T/C | — | uncertain significance |
| rs2536193829 | 8:77,616,396 | A/G | — | uncertain significance |
| rs1808179909 | 8:77,616,441 | C/T | — | uncertain significance |
| rs1339350986 | 8:77,616,447 | A/G | — | uncertain significance |
| rs1228195149 | 8:77,616,456 | A/C | — | uncertain significance |
| rs751341224 | 8:77,616,482 | G/C | — | likely benign |
| rs192355194 | 8:77,616,490 | G/A | — | uncertain significance |
| rs141168301 | 8:77,616,515 | C/T | — | benign |
| rs56261025 | 8:77,616,519 | G/C | — | benign |
| rs2536194070 | 8:77,616,523 | A/G | — | uncertain significance |
| rs541217165 | 8:77,616,557 | G/A | — | likely benign |
| rs754793159 | 8:77,616,564 | C/A | — | uncertain significance |
| rs1337501369 | 8:77,616,706 | C/G | — | uncertain significance |
| rs1386254149 | 8:77,616,760 | A/T | — | uncertain significance |
| rs769631578 | 8:77,616,770 | G/A | — | likely benign |
| rs374845482 | 8:77,616,801 | C/T | — | uncertain significance |
| rs147642461 | 8:77,616,813 | G/A | — | likely benign |
| rs770449887 | 8:77,616,873 | C/T | — | uncertain significance |
| rs2536194619 | 8:77,616,891 | C/G | — | uncertain significance |
| rs2536194625 | 8:77,616,895 | T/G | — | uncertain significance |
| rs191883247 | 8:77,616,920 | A/T | — | benign |
| rs751723912 | 8:77,616,932 | A/G | — | likely benign |
| rs1221204945 | 8:77,617,009 | T/C | — | uncertain significance |
| rs777703837 | 8:77,617,034 | G/T | — | uncertain significance |
| rs1178807555 | 8:77,617,097 | C/A | — | uncertain significance |
| rs369214100 | 8:77,617,133 | C/A | — | uncertain significance |
| rs372636732 | 8:77,617,149 | C/T | — | uncertain significance |
| rs888095047 | 8:77,617,169 | G/T | — | uncertain significance |
| rs2536195039 | 8:77,617,191 | A/G | — | uncertain significance |
| rs766005588 | 8:77,617,244 | C/G | — | likely benign |
| rs1585863819 | 8:77,617,265 | T/C | — | likely benign |
| rs2536195199 | 8:77,617,273 | G/A | — | uncertain significance |
| rs1808212197 | 8:77,617,276 | T/A | — | uncertain significance |
| rs749086451 | 8:77,617,309 | A/G | — | uncertain significance |
| rs770313841 | 8:77,617,353 | G/A | — | uncertain significance |
| rs373343766 | 8:77,617,355 | T/C | — | likely benign |
| rs2536195348 | 8:77,617,369 | C/T | — | uncertain significance |
| rs370676988 | 8:77,617,372 | C/A | — | uncertain significance |
| rs1808216376 | 8:77,617,380 | C/A | — | uncertain significance |
| rs376626064 | 8:77,617,399 | C/T | — | uncertain significance |
| rs778804692 | 8:77,617,442 | C/T | — | likely benign |
| rs184068009 | 8:77,617,452 | G/A | — | uncertain significance |
| rs746216359 | 8:77,617,486 | C/A | — | uncertain significance |
| rs372831335 | 8:77,617,492 | G/A | — | uncertain significance |
| rs189444720 | 8:77,617,500 | G/C | — | likely benign |
| rs372128559 | 8:77,617,600 | G/A | — | benign |
| rs751284629 | 8:77,617,609 | C/T | — | uncertain significance |
| rs577443909 | 8:77,617,710 | A/C | — | uncertain significance |
| rs775936557 | 8:77,617,736 | T/C | — | likely benign |
| rs953528643 | 8:77,617,782 | G/C | — | uncertain significance |
| rs73690865 | 8:77,617,798 | C/T | — | benign |
| rs140868075 | 8:77,617,820 | T/C | — | likely benign |
| rs868044465 | 8:77,617,926 | A/G | — | uncertain significance |
| rs879561961 | 8:77,618,050 | A/T | — | uncertain significance |
| rs573814554 | 8:77,618,060 | G/C | — | benign |
| rs1333886732 | 8:77,618,067 | G/A | — | uncertain significance |
| rs577863838 | 8:77,618,074 | G/C | — | uncertain significance |
| rs370086541 | 8:77,618,085 | C/A | — | uncertain significance |
| rs190829881 | 8:77,618,333 | G/T | — | likely benign |
| rs764242429 | 8:77,618,362 | G/A | — | uncertain significance |
| rs755122308 | 8:77,618,417 | C/T | — | likely benign |
| rs2536196852 | 8:77,618,434 | G/A | — | uncertain significance |
| rs2536196890 | 8:77,618,467 | G/A | — | uncertain significance |
| rs765118434 | 8:77,618,550 | G/T | — | uncertain significance |
| rs551678593 | 8:77,618,589 | C/T | — | uncertain significance |
| rs757841215 | 8:77,618,653 | A/G | — | uncertain significance |
| rs2536197175 | 8:77,618,731 | A/G | — | uncertain significance |
| rs1299909189 | 8:77,618,806 | A/G | — | uncertain significance |
| rs374480311 | 8:77,618,811 | G/C | — | uncertain significance |
| rs1017941003 | 8:77,618,815 | T/C | — | uncertain significance |
| rs201793372 | 8:77,619,778 | T/C | — | likely benign |
| rs765357495 | 8:77,619,788 | T/A | — | uncertain significance |
| rs61729525 | 8:77,619,861 | G/C | — | uncertain significance |
| rs764774396 | 8:77,619,951 | A/C | — | uncertain significance |
| rs745942387 | 8:77,620,045 | C/G | — | uncertain significance |
| rs1808320303 | 8:77,620,095 | C/T | — | uncertain significance |
| rs371959933 | 8:77,620,109 | G/C | — | likely benign |
| rs990934665 | 8:77,620,155 | A/C | — | uncertain significance |
| rs1453115693 | 8:77,620,176 | C/G | — | uncertain significance |
| rs376831938 | 8:77,620,196 | C/T | — | likely benign |
| rs369411377 | 8:77,620,197 | G/A | — | uncertain significance |
| rs767560522 | 8:77,620,246 | C/G | — | uncertain significance |
| rs750690709 | 8:77,620,259 | C/T | — | likely benign |
| rs376251060 | 8:77,620,265 | G/A | — | likely benign |
| rs7842138 | 8:77,632,017 | A/G | intron variant | — |
| rs1433965 | 8:77,633,344 | T/A | — | — |
| rs16939343 | 8:77,640,595 | T/A | — | — |
| rs11985148 | 8:77,643,348 | A/T | — | — |
| rs7822914 | 8:77,663,038 | C/T | intron variant | — |
| rs7821604 | 8:77,675,312 | C/T | — | — |
| rs76132822 | 8:77,679,194 | C/T | intron variant | — |
| rs749259046 | 8:77,690,483 | T/C | — | uncertain significance |
| rs144357822 | 8:77,690,500 | C/T | — | likely benign |
| rs370547889 | 8:77,690,524 | C/T | — | likely benign |
| rs750806468 | 8:77,690,550 | G/A | — | uncertain significance |
| rs16939357 | 8:77,690,563 | T/C | — | benign |
Showing 100 of 289 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.