| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123633611-123633856 | Common:1; Rare:118; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972541-123972905 | Common:6; Rare:123 | ||||
| chr12:123973008-123973303 | Common:2; Rare:97 | ||||
| chr12:124388808-124388934 | Common:3; Rare:38 | ||||
| chr12:124422614-124422977 | Common:4; Rare:90 | ||||
| chr12:124914063-124914199 | Common:7; Rare:57 | ||||
| chr12:124914567-124915061 | Common:9; Rare:205 | ||||
| chr12:128824038-128824089 | Rare:13 | ||||
| chr12:130871766-130872122 | Common:4; Rare:141 | ||||
| chr12:131710795-131711107 | Rare:82 | ||||
| chr12:131929001-131929296 | Common:10; Rare:89; Clinvar:1 | ||||
| chr12:131949626-131950014 | Common:2; Rare:130 | ||||
| chr12:132687311-132687713 | Common:4; Rare:149; Clinvar:5; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132710758-132710852 | Common:2; Rare:40 | ||||
| chr12:132829052-132829216 | Rare:78 |