| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:216271987-216272138 | Rare:21 | ||||
| chr2:216283401-216283721 | Common:2; Rare:68; Clinvar:1 | ||||
| chr2:216293584-216293821 | Common:4; Rare:25 | ||||
| chr2:216371218-216371292 | Rare:15 | ||||
| chr2:216372705-216372984 | Rare:50 | ||||
| chr2:216420066-216420324 | Common:2; Rare:43; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr2:216434878-216435140 | Rare:50 | ||||
| chr2:216611015-216611174 | Common:1; Rare:19 | ||||
| chr2:217223474-217223795 | Common:3; Rare:54 | ||||
| chr2:217239234-217239256 | Rare:1 | ||||
| chr2:217993171-217993351 | Common:4; Rare:21 | ||||
| chr2:218237547-218237878 | Common:4; Rare:55 | ||||
| chr2:218277406-218277669 | Rare:78 | ||||
| chr2:218295124-218295413 | Rare:56 | ||||
| chr2:218323976-218324170 | Common:3; Rare:42 |