| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109104558-109104766 | Common:4; Rare:45 | ||||
| chr12:110282599-110282796 | Rare:57; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:110283838-110283936 | Rare:18 | ||||
| chr12:111839840-111839938 | Rare:15 | ||||
| chr12:111888251-111888520 | Common:3; Rare:41 | ||||
| chr12:112029697-112029810 | Rare:14 | ||||
| chr12:112043790-112044086 | Common:2; Rare:55 | ||||
| chr12:112104562-112104812 | Common:3; Rare:38 | ||||
| chr12:113744472-113744689 | Common:1; Rare:37 | ||||
| chr12:116102637-116102781 | Common:14; Rare:43 | ||||
| chr12:116165418-116165620 | Common:1; Rare:47 | ||||
| chr12:116192679-116192833 | Common:2; Rare:25 | ||||
| chr12:116198361-116198542 | Common:2; Rare:34 | ||||
| chr12:116226260-116226373 | Rare:20 | ||||
| chr12:116368562-116368789 | Common:3; Rare:40 |