| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:55940368-55940589 | Common:2; Rare:56 | ||||
| chr12:55966037-55966239 | Common:1; Rare:37 | ||||
| chr12:55966631-55966882 | Rare:67 | ||||
| chr12:55966995-55967023 | Rare:11 | ||||
| chr12:55973444-55973478 | Rare:3 | ||||
| chr12:55973649-55974169 | Common:3; Rare:144 | ||||
| chr12:56007317-56007452 | Rare:21 | ||||
| chr12:56007721-56007996 | Common:2; Rare:62 | ||||
| chr12:56041543-56041926 | Common:3; Rare:83 | ||||
| chr12:56042087-56042246 | Common:2; Rare:82; Clinvar:1; Clinvar (benign):5 | ||||
| chr12:56042370-56042599 | Rare:65; Clinvar (benign):1 | ||||
| chr12:56079347-56079568 | Rare:43 | ||||
| chr12:56104124-56104732 | Common:5; Rare:206 | ||||
| chr12:56105083-56105261 | Rare:37 | ||||
| chr12:56105280-56105398 | Rare:20 |