| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109939309-109939357 | Rare:10 | ||||
| chr12:109996220-109996439 | Common:2; Rare:64 | ||||
| chr12:110281012-110281264 | Rare:92 | ||||
| chr12:110502047-110502332 | Common:1; Rare:103 | ||||
| chr12:110613997-110614269 | Rare:89; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:110742655-110742753 | Common:1; Rare:27; Clinvar:1 | ||||
| chr12:111368972-111369290 | Common:1; Rare:83 | ||||
| chr12:111598817-111598942 | Rare:40; Clinvar (pathogenic):1 | ||||
| chr12:111599291-111599635 | Common:2; Rare:115 | ||||
| chr12:111685776-111686168 | Rare:146 | ||||
| chr12:111766807-111767091 | Rare:89 | ||||
| chr12:111841867-111842060 | Common:2; Rare:56 | ||||
| chr12:111885775-111886034 | Common:1; Rare:58 | ||||
| chr12:111888628-111888996 | Common:1; Rare:73 | ||||
| chr12:112005947-112006151 | Common:3; Rare:30 |