| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:119178627-119178935 | Common:1; Rare:53; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:119668100-119668184 | Common:1; Rare:16 | ||||
| chr12:120116747-120116938 | Common:2; Rare:64 | ||||
| chr12:120201081-120201360 | Common:2; Rare:89 | ||||
| chr12:120446338-120446483 | Common:1; Rare:65 | ||||
| chr12:120469478-120469895 | Common:5; Rare:139 | ||||
| chr12:120495867-120496228 | Common:7; Rare:121 | ||||
| chr12:120581349-120581405 | Rare:33 | ||||
| chr12:121210088-121210152 | Rare:25 | ||||
| chr12:121296682-121296894 | Common:1; Rare:61 | ||||
| chr12:121802936-121803096 | Rare:36 | ||||
| chr12:122266404-122266584 | Common:2; Rare:67 | ||||
| chr12:122526864-122527282 | Common:4; Rare:147 | ||||
| chr12:122871114-122871182 | Rare:9 | ||||
| chr12:122975101-122975241 | Common:1; Rare:30 |