| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:140479323-140479650 | Rare:97 | ||||
| chr7:140924128-140924455 | Common:1; Rare:84 | ||||
| chr7:141551342-141551428 | Rare:24; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141737939-141738455 | Common:5; Rare:151 | ||||
| chr7:148884210-148884467 | Common:1; Rare:110; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:149028450-149028589 | Common:2; Rare:54 | ||||
| chr7:149090633-149090880 | Rare:75 | ||||
| chr7:149147095-149147141 | Rare:7 | ||||
| chr7:149147257-149147476 | Common:3; Rare:49 | ||||
| chr7:149250610-149250773 | Common:1; Rare:45 | ||||
| chr7:150368702-150368862 | Common:1; Rare:48 | ||||
| chr7:150368925-150369136 | Common:2; Rare:56 | ||||
| chr7:150405273-150405880 | Common:1; Rare:153 | ||||
| chr7:150685674-150685760 | Rare:15 | ||||
| chr7:151013802-151014000 | Common:1; Rare:86; Clinvar (benign):1 |