| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:215311901-215312133 | Common:8; Rare:95 | ||||
| chr2:215436037-215436225 | Common:2; Rare:66 | ||||
| chr2:216081761-216081911 | Common:1; Rare:51 | ||||
| chr2:216412217-216412538 | Common:2; Rare:73; Clinvar (benign):1 | ||||
| chr2:216412667-216412782 | Rare:13 | ||||
| chr2:216498689-216498904 | Common:7; Rare:92 | ||||
| chr2:218217040-218217262 | Common:1; Rare:75 | ||||
| chr2:218260728-218261023 | Rare:50 | ||||
| chr2:218269649-218269884 | Rare:63 | ||||
| chr2:218270091-218270602 | Common:5; Rare:165; Clinvar:6; Clinvar (benign):2 | ||||
| chr2:218287265-218287427 | Common:1; Rare:27 | ||||
| chr2:218322982-218323386 | Common:6; Rare:140 | ||||
| chr2:218398014-218398245 | Common:1; Rare:79 | ||||
| chr2:218398509-218398660 | Common:1; Rare:51 | ||||
| chr2:218399625-218399766 | Rare:67 |