| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:118061093-118061468 | Common:4; Rare:75 | ||||
| chr12:118103868-118104100 | Common:1; Rare:56 | ||||
| chr12:118135946-118136340 | Common:2; Rare:117 | ||||
| chr12:118372764-118373189 | Common:2; Rare:113 | ||||
| chr12:118376479-118376599 | Common:1; Rare:48 | ||||
| chr12:118376701-118376810 | Rare:33 | ||||
| chr12:119178669-119178959 | Common:1; Rare:49; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:119668094-119668184 | Common:1; Rare:18 | ||||
| chr12:120116622-120116917 | Common:3; Rare:78 | ||||
| chr12:120194683-120194755 | Rare:27 | ||||
| chr12:120197459-120197627 | Common:2; Rare:47 | ||||
| chr12:120200710-120201374 | Common:3; Rare:217 | ||||
| chr12:120437842-120438132 | Common:2; Rare:88; Clinvar (benign):1 | ||||
| chr12:120446226-120446491 | Common:2; Rare:98 | ||||
| chr12:120469709-120469868 | Common:1; Rare:49 |