| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:141014617-141014744 | Rare:22 | ||||
| chr7:141551265-141551434 | Common:1; Rare:48; Clinvar:5; Clinvar (benign):2 | ||||
| chr7:141738021-141738632 | Common:5; Rare:169 | ||||
| chr7:143288051-143288442 | Common:2; Rare:133 | ||||
| chr7:144355185-144355478 | Rare:2 | ||||
| chr7:148339146-148339529 | Common:9; Rare:90 | ||||
| chr7:148698360-148698657 | Common:5; Rare:92 | ||||
| chr7:149028646-149028955 | Common:1; Rare:99 | ||||
| chr7:149090672-149090907 | Rare:63 | ||||
| chr7:149126234-149126438 | Common:6; Rare:68 | ||||
| chr7:149873804-149874048 | Common:3; Rare:97 | ||||
| chr7:150323414-150323517 | Common:1; Rare:27 | ||||
| chr7:150368776-150368889 | Rare:38 | ||||
| chr7:150379061-150379335 | Common:2; Rare:98 | ||||
| chr7:150800307-150800827 | Common:7; Rare:134 |