| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:148698461-148699010 | Common:6; Rare:185 | ||||
| chr7:148884102-148884480 | Common:1; Rare:165; Clinvar:3; Clinvar (benign):1 | ||||
| chr7:149028389-149028606 | Common:3; Rare:84 | ||||
| chr7:149028613-149028884 | Common:3; Rare:97 | ||||
| chr7:149090656-149090915 | Rare:73 | ||||
| chr7:149126220-149126475 | Common:7; Rare:90 | ||||
| chr7:149261934-149262237 | Common:2; Rare:101 | ||||
| chr7:149714674-149714996 | Common:3; Rare:101 | ||||
| chr7:149873823-149874123 | Common:3; Rare:108 | ||||
| chr7:150368665-150368889 | Common:1; Rare:75 | ||||
| chr7:150368923-150369149 | Common:2; Rare:58 | ||||
| chr7:150379057-150379365 | Common:2; Rare:111 | ||||
| chr7:151028149-151028498 | Rare:127 | ||||
| chr7:151028700-151028755 | Rare:11 | ||||
| chr7:151057844-151058205 | Common:3; Rare:105 |