| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:141739015-141739298 | Common:3; Rare:59 | ||||
| chr3:141797288-141797450 | Rare:40 | ||||
| chr3:141797488-141798001 | Common:1; Rare:119 | ||||
| chr3:142027451-142028062 | Common:5; Rare:157 | ||||
| chr3:143887736-143888550 | Common:6; Rare:185 | ||||
| chr3:143897928-143898237 | Rare:76 | ||||
| chr3:144549311-144549447 | Rare:22 | ||||
| chr3:146582137-146582537 | Common:5; Rare:99 | ||||
| chr3:146610716-146611116 | Rare:105 | ||||
| chr3:146625786-146626259 | Common:3; Rare:114 | ||||
| chr3:147423147-147423798 | Common:2; Rare:186 | ||||
| chr3:147939569-147940201 | Common:4; Rare:265 | ||||
| chr3:148643326-148643730 | Common:3; Rare:137 | ||||
| chr3:148742193-148742328 | Common:2; Rare:33; Clinvar (benign):2 | ||||
| chr3:148789129-148789529 | Common:5; Rare:112 |