| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:27645918-27646096 | Common:1; Rare:54 | ||||
| chr12:27898243-27898368 | Common:1; Rare:20 | ||||
| chr12:29744152-29744188 | Rare:6 | ||||
| chr12:30662426-30662732 | Common:2; Rare:53 | ||||
| chr12:30796178-30796198 | Rare:5 | ||||
| chr12:31518809-31519090 | Common:3; Rare:41 | ||||
| chr12:32218289-32218539 | Common:1; Rare:37 | ||||
| chr12:32736991-32737161 | Common:1; Rare:38; Clinvar (pathogenic):1 | ||||
| chr12:34236233-34236250 | Common:1 | ||||
| chr12:42313697-42313970 | Common:1; Rare:82 | ||||
| chr12:42313974-42314272 | Common:1; Rare:42 | ||||
| chr12:42498758-42498946 | Common:2; Rare:33 | ||||
| chr12:42513590-42513894 | Common:1; Rare:48 | ||||
| chr12:42515323-42515525 | Common:4; Rare:40 | ||||
| chr12:42526322-42526450 | Rare:15 |