| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:141551265-141551423 | Common:1; Rare:47; Clinvar:5; Clinvar (benign):2 | ||||
| chr7:141737986-141738464 | Common:4; Rare:142 | ||||
| chr7:142854990-142855133 | Common:2; Rare:42 | ||||
| chr7:143288165-143288442 | Common:1; Rare:105 | ||||
| chr7:143380955-143381061 | Rare:27 | ||||
| chr7:144835997-144836149 | Rare:50 | ||||
| chr7:148698360-148698748 | Common:5; Rare:121 | ||||
| chr7:149028374-149028616 | Common:4; Rare:95 | ||||
| chr7:149090662-149090876 | Rare:60 | ||||
| chr7:149126234-149126438 | Common:6; Rare:68 | ||||
| chr7:150379081-150379335 | Common:1; Rare:86 | ||||
| chr7:150567294-150567428 | Rare:20 | ||||
| chr7:150800296-150800818 | Common:7; Rare:135 | ||||
| chr7:150993530-150993779 | Common:2; Rare:59 | ||||
| chr7:151059464-151059716 | Common:1; Rare:75 |