| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:140696602-140696756 | Common:1; Rare:56 | ||||
| chr7:141014638-141014744 | Rare:17 | ||||
| chr7:141014924-141015134 | Rare:51 | ||||
| chr7:141551342-141551434 | Rare:24; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141738021-141738484 | Common:4; Rare:136 | ||||
| chr7:142854990-142855202 | Common:3; Rare:60 | ||||
| chr7:143263404-143263511 | Rare:31 | ||||
| chr7:143288150-143288442 | Common:1; Rare:107 | ||||
| chr7:143380978-143381330 | Common:1; Rare:110 | ||||
| chr7:143902121-143902304 | Common:5; Rare:58 | ||||
| chr7:144835989-144836126 | Rare:40 | ||||
| chr7:148698337-148698973 | Common:6; Rare:212 | ||||
| chr7:149028362-149028577 | Common:2; Rare:84 | ||||
| chr7:149028581-149028700 | Common:5; Rare:54 | ||||
| chr7:149090657-149090857 | Rare:60 |