| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:118135955-118136175 | Common:2; Rare:69 | ||||
| chr12:118372820-118373220 | Common:2; Rare:113 | ||||
| chr12:119667854-119668089 | Common:2; Rare:59 | ||||
| chr12:119668093-119668194 | Common:1; Rare:20 | ||||
| chr12:120116641-120116935 | Common:5; Rare:84 | ||||
| chr12:120201081-120201319 | Common:2; Rare:78 | ||||
| chr12:120437888-120438222 | Common:2; Rare:127; Clinvar (benign):2 | ||||
| chr12:120446321-120446495 | Common:2; Rare:77 | ||||
| chr12:120469454-120469889 | Common:6; Rare:142 | ||||
| chr12:120495845-120496214 | Common:7; Rare:127 | ||||
| chr12:121209890-121210156 | Common:5; Rare:82 | ||||
| chr12:121399885-121400165 | Common:5; Rare:103 | ||||
| chr12:121580997-121581115 | Rare:17 | ||||
| chr12:121802926-121803091 | Rare:42 | ||||
| chr12:121918451-121918610 | Common:5; Rare:34 |