EBF1
EBF transcription factor 1
Summary
Predicted to enable DNA-binding transcription activator activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in positive regulation of transcription by RNA polymerase II. Predicted to act upstream of or within positive regulation of DNA-templated transcription. Predicted to be located in chromatin. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants57 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1758270832 | 5:158,135,019 | G/T | — | uncertain significance |
| rs764892787 | 5:158,135,047 | C/T | — | uncertain significance |
| rs1446440015 | 5:158,135,086 | C/T | — | uncertain significance |
| rs748539172 | 5:158,139,165 | C/T | — | uncertain significance |
| rs267600518 | 5:158,139,263 | G/C | — | uncertain significance |
| rs913725865 | 5:158,139,318 | C/T | — | uncertain significance |
| rs1010503968 | 5:158,139,983 | T/C | — | uncertain significance |
| rs1170847073 | 5:158,139,996 | A/G | — | uncertain significance |
| rs149065953 | 5:158,140,041 | C/T | — | uncertain significance |
| rs762145923 | 5:158,140,073 | G/A | — | uncertain significance |
| rs774052785 | 5:158,140,082 | G/A | — | uncertain significance |
| rs755850355 | 5:158,140,100 | C/A | — | uncertain significance |
| rs13170526 | 5:158,175,669 | T/G | intron variant | — |
| rs6863275 | 5:158,196,742 | A/G | — | — |
| rs2533645694 | 5:158,204,469 | T/G | — | uncertain significance |
| rs10079275 | 5:158,208,270 | A/G | — | — |
| rs6860231 | 5:158,223,090 | C/T | intron variant | — |
| rs2534005098 | 5:158,223,414 | A/G | — | uncertain significance |
| rs1432679 | 5:158,244,083 | C/T | intron variant | — |
| rs4704780 | 5:158,246,785 | A/C | intron variant | — |
| rs4704963 | 5:158,247,378 | T/A | — | — |
| rs144663267 | 5:158,250,294 | C/T | — | uncertain significance |
| rs17056278 | 5:158,252,438 | C/T | — | — |
| rs1368297 | 5:158,255,046 | T/A | intron variant | — |
| rs6876405 | 5:158,263,480 | T/G | intron variant | — |
| rs112824187 | 5:158,265,308 | G/T | — | — |
| rs749897481 | 5:158,267,048 | G/A | — | uncertain significance |
| rs4594837 | 5:158,267,974 | A/T | — | — |
| rs80330977 | 5:158,276,610 | G/T | — | — |
| rs77239429 | 5:158,305,074 | A/T | intron variant | — |
| rs536115678 | 5:158,311,343 | C/T | — | — |
| rs75512885 | 5:158,317,602 | T/C | — | — |
| rs1422798 | 5:158,320,877 | C/G | intron variant | — |
| rs62385378 | 5:158,327,312 | G/A | intron variant | — |
| rs17658268 | 5:158,328,181 | T/C | intron variant | — |
| rs62385385 | 5:158,367,249 | T/A | intron variant | — |
| rs7443323 | 5:158,368,797 | T/A | intron variant | — |
| rs35003579 | 5:158,378,341 | G/A | intron variant | — |
| rs191406954 | 5:158,395,728 | T/C | intron variant | — |
| rs7380908 | 5:158,396,062 | A/C | intron variant | — |
| rs149148360 | 5:158,417,225 | C/T | downstream gene variant | — |
| rs10040979 | 5:158,424,391 | G/A | intron variant | — |
| rs4921518 | 5:158,432,457 | A/C | — | — |
| rs67265526 | 5:158,433,339 | T/C | intron variant | — |
| rs77581390 | 5:158,433,563 | G/A | intron variant | — |
| rs6862399 | 5:158,441,675 | G/T | intron variant | — |
| rs36071027 | 5:158,444,274 | C/T | intron variant | — |
| rs72813940 | 5:158,477,980 | T/C | regulatory region variant | — |
| rs7705707 | 5:158,480,615 | A/T | intron variant | — |
| rs6865969 | 5:158,502,728 | T/A | — | — |
| rs10515789 | 5:158,506,415 | T/G | intron variant | — |
| rs1422669 | 5:158,507,655 | T/C | intron variant | — |
| rs1782462401 | 5:158,522,641 | G/T | — | uncertain significance |
| rs2535905896 | 5:158,522,642 | A/T | — | uncertain significance |
| rs201413959 | 5:158,522,674 | G/A | — | uncertain significance |
| rs6895454 | 5:158,523,167 | C/T | upstream gene variant | — |
| rs756741736 | 5:158,526,372 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.