| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74503306-74503476 | Rare:72 | ||||
| chr2:74507337-74507545 | Rare:104 | ||||
| chr2:74507600-74507900 | Common:1; Rare:116 | ||||
| chr2:74528920-74529590 | Common:6; Rare:328; Clinvar (benign):4 | ||||
| chr2:74529665-74530161 | Rare:251; Clinvar:6; Clinvar (benign):2 | ||||
| chr2:74530757-74530962 | Rare:98 | ||||
| chr2:74548560-74549126 | Common:1; Rare:163 | ||||
| chr2:74654020-74654380 | Common:3; Rare:212 | ||||
| chr2:74833824-74834190 | Common:1; Rare:199 | ||||
| chr2:74835141-74835300 | Rare:44 | ||||
| chr2:74835234-74835355 | Common:1; Rare:27 | ||||
| chr2:74958385-74958707 | Common:9; Rare:164 | ||||
| chr2:74958870-74959071 | Rare:134 | ||||
| chr2:75646615-75646825 | Rare:102 | ||||
| chr2:75710614-75710814 | Common:4; Rare:148 |