| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:125375243-125375391 | Rare:40 | ||||
| chr3:127598223-127598432 | Common:3; Rare:52 | ||||
| chr3:128052186-128052543 | Common:2; Rare:122 | ||||
| chr3:128879408-128879676 | Common:4; Rare:130; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:129183794-129184012 | Common:2; Rare:68 | ||||
| chr3:129249545-129249675 | Common:1; Rare:41 | ||||
| chr3:129439847-129440366 | Common:1; Rare:159; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:129893591-129893875 | Rare:126 | ||||
| chr3:130893905-130894253 | Common:3; Rare:101 | ||||
| chr3:131026749-131026940 | Common:2; Rare:50 | ||||
| chr3:131381432-131381805 | Common:3; Rare:92 | ||||
| chr3:133661863-133662004 | Rare:32 | ||||
| chr3:134485699-134485766 | Rare:28 | ||||
| chr3:134485957-134486229 | Common:2; Rare:93 | ||||
| chr3:136862064-136862277 | Rare:57 |