| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:108562388-108562651 | Common:6; Rare:104; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:108731513-108731680 | Common:2; Rare:63 | ||||
| chr12:109097967-109098244 | Common:4; Rare:89 | ||||
| chr12:109477287-109477641 | Common:3; Rare:86 | ||||
| chr12:109573485-109573845 | Common:3; Rare:101; Clinvar:4; Clinvar (benign):5 | ||||
| chr12:110468671-110468909 | Rare:59 | ||||
| chr12:111841887-111841983 | Common:1; Rare:28 | ||||
| chr12:112013135-112013460 | Common:1; Rare:111 | ||||
| chr12:113185435-113185748 | Common:7; Rare:118 | ||||
| chr12:113966294-113966504 | Common:7; Rare:72 | ||||
| chr12:118016577-118016806 | Common:1; Rare:48 | ||||
| chr12:118135955-118136175 | Common:2; Rare:69 | ||||
| chr12:119877266-119877557 | Common:2; Rare:64 | ||||
| chr12:120194693-120194787 | Rare:34 | ||||
| chr12:120201081-120201354 | Common:2; Rare:88 |