| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:72334956-72335111 | Rare:41 | ||||
| chr2:72825825-72826128 | Rare:92 | ||||
| chr2:73071685-73071857 | Common:2; Rare:69 | ||||
| chr2:73214483-73214597 | Common:1; Rare:44 | ||||
| chr2:73233193-73233451 | Common:1; Rare:67 | ||||
| chr2:73234140-73234368 | Common:2; Rare:65 | ||||
| chr2:73284277-73284476 | Common:1; Rare:52 | ||||
| chr2:73385641-73386076 | Common:4; Rare:204; Clinvar:16; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr2:73386118-73386339 | Common:1; Rare:83; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:73737266-73737547 | Common:3; Rare:91 | ||||
| chr2:73780012-73780254 | Common:1; Rare:98 | ||||
| chr2:73828794-73829037 | Common:1; Rare:55 | ||||
| chr2:74002568-74002730 | Common:2; Rare:66 | ||||
| chr2:74147830-74148161 | Common:3; Rare:87; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74148298-74148478 | Common:2; Rare:40 |