| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57772079-57772258 | Rare:62 | ||||
| chr12:57772516-57772676 | Common:3; Rare:23 | ||||
| chr12:57846392-57846502 | Rare:33 | ||||
| chr12:57846903-57847221 | Common:2; Rare:114 | ||||
| chr12:57941360-57941704 | Common:3; Rare:102 | ||||
| chr12:57941740-57941801 | Rare:16 | ||||
| chr12:59595862-59596207 | Common:5; Rare:77 | ||||
| chr12:62260044-62260441 | Common:1; Rare:149 | ||||
| chr12:63149870-63149881 | Rare:3 | ||||
| chr12:63149887-63150294 | Common:1; Rare:136 | ||||
| chr12:63150639-63151276 | Common:3; Rare:180 | ||||
| chr12:63668459-63668665 | Rare:56 | ||||
| chr12:63779749-63779921 | Common:2; Rare:61; Clinvar (benign):1 | ||||
| chr12:63780087-63780184 | Rare:45; Clinvar (pathogenic):1 | ||||
| chr12:63844762-63844812 | Rare:16 |