| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:70086931-70087071 | Common:1; Rare:74 | ||||
| chr2:70087276-70087589 | Common:3; Rare:109 | ||||
| chr2:70293659-70294059 | Common:4; Rare:106 | ||||
| chr2:71068533-71068648 | Rare:54 | ||||
| chr2:71130225-71130659 | Common:6; Rare:120; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:73233200-73233522 | Common:1; Rare:94 | ||||
| chr2:73234201-73234357 | Common:2; Rare:46 | ||||
| chr2:73284256-73284531 | Common:1; Rare:68 | ||||
| chr2:73737304-73737565 | Common:3; Rare:87 | ||||
| chr2:73828804-73829043 | Common:1; Rare:58 | ||||
| chr2:73926689-73926926 | Common:2; Rare:110; Clinvar:6; Clinvar (benign):2 | ||||
| chr2:74147870-74148056 | Common:1; Rare:48; Clinvar:2 | ||||
| chr2:74178800-74179070 | Common:4; Rare:84 | ||||
| chr2:74198440-74198643 | Rare:84 | ||||
| chr2:74421562-74421786 | Rare:74 |