| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:118135938-118136195 | Common:2; Rare:80 | ||||
| chr12:118372820-118373199 | Common:2; Rare:104 | ||||
| chr12:118376211-118376592 | Common:1; Rare:114 | ||||
| chr12:119178538-119179109 | Common:2; Rare:106; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:119668105-119668180 | Common:1; Rare:14 | ||||
| chr12:120116712-120116935 | Common:3; Rare:74 | ||||
| chr12:120194690-120194786 | Rare:34 | ||||
| chr12:120201083-120201380 | Common:2; Rare:95 | ||||
| chr12:120250002-120250277 | Common:2; Rare:43 | ||||
| chr12:120446353-120446495 | Common:2; Rare:67 | ||||
| chr12:120469575-120469889 | Common:3; Rare:110 | ||||
| chr12:120495845-120496229 | Common:7; Rare:128 | ||||
| chr12:120497823-120498114 | Rare:61 | ||||
| chr12:120529093-120529188 | Common:2; Rare:41 | ||||
| chr12:120534545-120534600 | Common:2; Rare:13 |