| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:110468702-110468915 | Rare:56 | ||||
| chr12:110502058-110502195 | Common:1; Rare:51 | ||||
| chr12:111685769-111686085 | Rare:119 | ||||
| chr12:111766794-111766973 | Rare:54 | ||||
| chr12:111841894-111842219 | Common:3; Rare:90 | ||||
| chr12:112013129-112013468 | Common:1; Rare:119 | ||||
| chr12:113185451-113185794 | Common:8; Rare:118 | ||||
| chr12:113966309-113966520 | Common:8; Rare:71 | ||||
| chr12:114408058-114408274 | Common:2; Rare:38; Clinvar (benign):3 | ||||
| chr12:114683964-114684036 | Rare:9 | ||||
| chr12:114684139-114684350 | Rare:54 | ||||
| chr12:114684497-114684631 | Rare:39 | ||||
| chr12:118135960-118136192 | Common:2; Rare:69 | ||||
| chr12:118372887-118373165 | Common:1; Rare:63 | ||||
| chr12:120116720-120116911 | Rare:58 |