| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57087837-57087952 | Common:1; Rare:32 | ||||
| chr12:57111180-57111420 | Common:4; Rare:46 | ||||
| chr12:57128332-57128872 | Common:1; Rare:101 | ||||
| chr12:57128953-57129018 | Rare:16 | ||||
| chr12:57201496-57201866 | Common:2; Rare:88 | ||||
| chr12:57233728-57233760 | Common:1; Rare:12 | ||||
| chr12:57520501-57520720 | Common:1; Rare:65 | ||||
| chr12:57610026-57610314 | Common:3; Rare:78 | ||||
| chr12:57772087-57772215 | Rare:48 | ||||
| chr12:57772539-57772626 | Common:2; Rare:10 | ||||
| chr12:57846926-57847221 | Common:2; Rare:109 | ||||
| chr12:62260056-62260452 | Common:1; Rare:149 | ||||
| chr12:64452011-64452174 | Common:1; Rare:61 | ||||
| chr12:64759109-64759472 | Rare:115; Clinvar:6; Clinvar (benign):2 | ||||
| chr12:65169452-65169616 | Common:1; Rare:58; Clinvar:2 |