| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:141014909-141015111 | Rare:44 | ||||
| chr7:141551238-141551434 | Common:3; Rare:53; Clinvar:5; Clinvar (benign):2 | ||||
| chr7:141738161-141738491 | Rare:115 | ||||
| chr7:142854990-142855138 | Common:2; Rare:44 | ||||
| chr7:143263320-143263532 | Rare:66 | ||||
| chr7:143288274-143288442 | Common:1; Rare:68 | ||||
| chr7:143380921-143381340 | Common:1; Rare:128 | ||||
| chr7:143902078-143902292 | Common:7; Rare:68 | ||||
| chr7:144835983-144836123 | Common:1; Rare:41; Clinvar (benign):1 | ||||
| chr7:148698575-148698965 | Common:3; Rare:139 | ||||
| chr7:148884213-148884474 | Common:1; Rare:112; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:149028350-149028556 | Common:2; Rare:77 | ||||
| chr7:149028581-149028938 | Common:5; Rare:120 | ||||
| chr7:149090657-149090908 | Rare:70 | ||||
| chr7:149126220-149126439 | Common:6; Rare:73 |