| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:143263338-143263532 | Rare:62 | ||||
| chr7:143288051-143288451 | Common:2; Rare:135 | ||||
| chr7:143380978-143381293 | Common:1; Rare:101 | ||||
| chr7:143408815-143408961 | Rare:34 | ||||
| chr7:143902068-143902283 | Common:7; Rare:66 | ||||
| chr7:144355162-144355478 | Rare:2 | ||||
| chr7:144835977-144836140 | Common:1; Rare:51; Clinvar (benign):1 | ||||
| chr7:148698569-148699002 | Common:4; Rare:153 | ||||
| chr7:148884219-148884464 | Common:1; Rare:103; Clinvar:1; Clinvar (benign):1 | ||||
| chr7:149028319-149028689 | Common:7; Rare:151 | ||||
| chr7:149028691-149028913 | Rare:63 | ||||
| chr7:149090656-149090876 | Rare:65 | ||||
| chr7:149126234-149126439 | Common:6; Rare:68 | ||||
| chr7:149147262-149147443 | Common:3; Rare:41 | ||||
| chr7:149261915-149262196 | Common:2; Rare:84 |