| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:68686814-68687000 | Common:4; Rare:52 | ||||
| chr12:69470304-69470425 | Common:2; Rare:41 | ||||
| chr12:69585308-69585506 | Common:3; Rare:80 | ||||
| chr12:74537717-74537855 | Rare:53 | ||||
| chr12:75390912-75391105 | Common:1; Rare:59 | ||||
| chr12:76084585-76084851 | Common:1; Rare:87 | ||||
| chr12:76348382-76348570 | Common:2; Rare:60; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:76764059-76764272 | Common:1; Rare:89 | ||||
| chr12:79934904-79935255 | Common:1; Rare:132 | ||||
| chr12:80937670-80937852 | Common:1; Rare:56 | ||||
| chr12:82358361-82358546 | Rare:77 | ||||
| chr12:82358748-82358875 | Common:3; Rare:66 | ||||
| chr12:82686715-82686960 | Common:1; Rare:84 | ||||
| chr12:85036265-85036371 | Rare:29 | ||||
| chr12:88142032-88142368 | Rare:92; Clinvar:3 |