| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:110281681-110281744 | Rare:16; Clinvar:1 | ||||
| chr12:110450254-110450437 | Common:2; Rare:69 | ||||
| chr12:110468667-110468909 | Rare:60 | ||||
| chr12:110502051-110502331 | Common:1; Rare:101 | ||||
| chr12:110613991-110614187 | Rare:57; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:110742869-110743217 | Common:2; Rare:114 | ||||
| chr12:111599590-111599658 | Common:1; Rare:30 | ||||
| chr12:111685737-111686110 | Rare:135 | ||||
| chr12:111841854-111842058 | Common:2; Rare:60 | ||||
| chr12:112013123-112013582 | Common:1; Rare:171 | ||||
| chr12:112013586-112013636 | Rare:18 | ||||
| chr12:112013875-112014103 | Rare:52 | ||||
| chr12:112108725-112108888 | Common:1; Rare:40 | ||||
| chr12:112409141-112409246 | Rare:19 | ||||
| chr12:112409409-112409707 | Common:1; Rare:92 |