| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:141014632-141014744 | Rare:17 | ||||
| chr7:141551265-141551434 | Common:1; Rare:48; Clinvar:5; Clinvar (benign):2 | ||||
| chr7:141737997-141738493 | Common:4; Rare:146 | ||||
| chr7:142854990-142855249 | Common:6; Rare:64 | ||||
| chr7:143288084-143288451 | Common:2; Rare:122 | ||||
| chr7:143380880-143381330 | Common:2; Rare:132 | ||||
| chr7:144835973-144836126 | Common:1; Rare:45; Clinvar (benign):1 | ||||
| chr7:148698475-148698986 | Common:5; Rare:177 | ||||
| chr7:149028362-149028938 | Common:7; Rare:205 | ||||
| chr7:149090657-149090930 | Rare:77 | ||||
| chr7:149126220-149126439 | Common:6; Rare:73 | ||||
| chr7:149261893-149262237 | Common:2; Rare:109 | ||||
| chr7:149872852-149872971 | Common:1; Rare:23 | ||||
| chr7:149873852-149874096 | Common:3; Rare:90 | ||||
| chr7:150323141-150323353 | Common:5; Rare:60 |