| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:207529786-207530132 | Common:2; Rare:93 | ||||
| chr2:207596795-207597052 | Common:2; Rare:40 | ||||
| chr2:207625090-207625403 | Common:2; Rare:94 | ||||
| chr2:208025458-208025589 | Common:2; Rare:35 | ||||
| chr2:208254047-208254377 | Common:1; Rare:67 | ||||
| chr2:208255019-208255255 | Common:2; Rare:63 | ||||
| chr2:208266032-208266095 | Common:3; Rare:26 | ||||
| chr2:208266111-208266396 | Common:6; Rare:96; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:209423793-209424113 | Common:1; Rare:95 | ||||
| chr2:209424163-209424252 | Rare:21 | ||||
| chr2:210170631-210170901 | Common:1; Rare:99 | ||||
| chr2:210171230-210171527 | Common:4; Rare:111 | ||||
| chr2:210225078-210225203 | Rare:37 | ||||
| chr2:210225251-210225494 | Rare:53; Clinvar:1 | ||||
| chr2:210225564-210225615 | Rare:10 |