| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:143119540-143119900 | Common:1; Rare:112 | ||||
| chr3:143971291-143971476 | Common:1; Rare:71 | ||||
| chr3:143971684-143971852 | Common:2; Rare:81 | ||||
| chr3:143971929-143972165 | Common:2; Rare:98 | ||||
| chr3:146544599-146544888 | Common:3; Rare:71 | ||||
| chr3:147409076-147409476 | Rare:180 | ||||
| chr3:148991160-148991630 | Common:7; Rare:175; Clinvar (benign):1 | ||||
| chr3:149086198-149086330 | Common:1; Rare:41 | ||||
| chr3:149086467-149086746 | Rare:86 | ||||
| chr3:149129447-149129721 | Common:3; Rare:117; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:149657468-149657588 | Common:1; Rare:19 | ||||
| chr3:149658014-149658209 | Rare:48 | ||||
| chr3:149752388-149752643 | Common:3; Rare:90 | ||||
| chr3:149792666-149793066 | Common:5; Rare:88 | ||||
| chr3:149812575-149812725 | Common:1; Rare:57 |