| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:141014628-141014744 | Rare:18 | ||||
| chr7:141551342-141551434 | Rare:24; Clinvar:4; Clinvar (benign):2 | ||||
| chr7:141738196-141738464 | Rare:100 | ||||
| chr7:142854990-142855133 | Common:2; Rare:42 | ||||
| chr7:143380931-143381368 | Common:1; Rare:137 | ||||
| chr7:144835972-144836139 | Common:1; Rare:51; Clinvar (benign):1 | ||||
| chr7:148698573-148698985 | Common:4; Rare:146 | ||||
| chr7:149126222-149126438 | Common:6; Rare:72 | ||||
| chr7:149873823-149874006 | Common:2; Rare:71 | ||||
| chr7:150379061-150379371 | Common:2; Rare:112 | ||||
| chr7:150405200-150405303 | Rare:23 | ||||
| chr7:150450517-150450859 | Common:1; Rare:74 | ||||
| chr7:150800315-150800447 | Common:3; Rare:32 | ||||
| chr7:151057856-151058200 | Common:3; Rare:98 | ||||
| chr7:151080785-151080920 | Rare:41 |