| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6568175-6568369 | Common:1; Rare:61 | ||||
| chr12:6581037-6581411 | Rare:125; Clinvar (pathogenic):2 | ||||
| chr12:6591449-6591828 | Rare:84 | ||||
| chr12:6592392-6592733 | Rare:64 | ||||
| chr12:6635922-6635974 | Rare:12 | ||||
| chr12:6689086-6689735 | Common:3; Rare:179 | ||||
| chr12:6723848-6724453 | Common:4; Rare:134 | ||||
| chr12:6752923-6753034 | Common:1; Rare:24 | ||||
| chr12:6753038-6753180 | Common:4; Rare:48 | ||||
| chr12:6766094-6767041 | Common:3; Rare:240 | ||||
| chr12:6828009-6828232 | Common:2; Rare:35 | ||||
| chr12:6828359-6828438 | Common:3; Rare:16 | ||||
| chr12:6851239-6851417 | Rare:43 | ||||
| chr12:6851913-6852224 | Rare:79 | ||||
| chr12:6868787-6868878 | Rare:32; Clinvar (pathogenic):1 |