| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:143902109-143902317 | Common:5; Rare:63 | ||||
| chr7:148698579-148698965 | Common:2; Rare:138 | ||||
| chr7:148884182-148884464 | Common:1; Rare:128; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:149028586-149028938 | Common:5; Rare:119 | ||||
| chr7:149126270-149126438 | Common:6; Rare:52 | ||||
| chr7:149195319-149195636 | Rare:77 | ||||
| chr7:149239474-149239698 | Common:2; Rare:58 | ||||
| chr7:149261893-149262218 | Common:2; Rare:106 | ||||
| chr7:150341587-150341824 | Common:1; Rare:28 | ||||
| chr7:150368518-150368867 | Common:1; Rare:99 | ||||
| chr7:150379057-150379365 | Common:2; Rare:111 | ||||
| chr7:151028246-151028493 | Rare:98 | ||||
| chr7:151057851-151058137 | Common:3; Rare:83 | ||||
| chr7:151058413-151058517 | Rare:11 | ||||
| chr7:151059487-151059716 | Common:1; Rare:68 |