| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:141014628-141014973 | Rare:75 | ||||
| chr7:141551318-141551428 | Rare:34; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141737956-141738489 | Common:5; Rare:155 | ||||
| chr7:142854775-142855133 | Common:9; Rare:105 | ||||
| chr7:143263327-143263576 | Rare:79 | ||||
| chr7:143288282-143288442 | Common:1; Rare:67 | ||||
| chr7:143380954-143381093 | Rare:40 | ||||
| chr7:143902109-143902304 | Common:5; Rare:61 | ||||
| chr7:144835989-144836106 | Rare:35 | ||||
| chr7:148698552-148699028 | Common:5; Rare:163 | ||||
| chr7:148884213-148884480 | Common:1; Rare:117; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:149090656-149090907 | Rare:71 | ||||
| chr7:149126234-149126453 | Common:6; Rare:75 | ||||
| chr7:149714670-149714992 | Common:3; Rare:103 | ||||
| chr7:149873694-149874056 | Common:4; Rare:127 |