| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:118061044-118061272 | Common:1; Rare:67 | ||||
| chr12:118061386-118061466 | Common:1; Rare:14 | ||||
| chr12:118135938-118136226 | Common:2; Rare:93 | ||||
| chr12:118139195-118139544 | Common:2; Rare:74 | ||||
| chr12:118189814-118190197 | Rare:80 | ||||
| chr12:118190428-118190634 | Common:1; Rare:39 | ||||
| chr12:118372815-118373192 | Common:2; Rare:102 | ||||
| chr12:118981279-118981576 | Common:1; Rare:87 | ||||
| chr12:119178849-119179122 | Common:2; Rare:43; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:119667670-119667983 | Common:2; Rare:83 | ||||
| chr12:119803465-119803562 | Rare:20 | ||||
| chr12:119857656-119857728 | Rare:18 | ||||
| chr12:119877266-119877526 | Common:2; Rare:57 | ||||
| chr12:120116608-120116943 | Common:5; Rare:92 | ||||
| chr12:120194693-120194785 | Rare:33 |