| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr7:144355393-144355469 | |||||
| chr7:144835976-144836106 | Common:1; Rare:39; Clinvar (benign):1 | ||||
| chr7:148698573-148699000 | Common:4; Rare:151 | ||||
| chr7:149028402-149028573 | Common:2; Rare:69 | ||||
| chr7:149028632-149028938 | Common:2; Rare:99 | ||||
| chr7:149090662-149090870 | Rare:59 | ||||
| chr7:149126220-149126432 | Common:6; Rare:72 | ||||
| chr7:149261911-149262267 | Common:3; Rare:110 | ||||
| chr7:149714670-149715051 | Common:4; Rare:123 | ||||
| chr7:149873863-149874048 | Common:3; Rare:78 | ||||
| chr7:150323188-150323353 | Common:5; Rare:46 | ||||
| chr7:150341579-150341898 | Common:2; Rare:47 | ||||
| chr7:150368702-150368905 | Common:1; Rare:59 | ||||
| chr7:150379061-150379371 | Common:2; Rare:112 | ||||
| chr7:150567291-150567428 | Rare:20 |