| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:128823957-128824089 | Rare:39 | ||||
| chr12:130839070-130839142 | Common:1; Rare:17 | ||||
| chr12:130871771-130872123 | Common:4; Rare:141 | ||||
| chr12:131929074-131929592 | Common:10; Rare:134; Clinvar:5; Clinvar (benign):1 | ||||
| chr12:132144310-132144503 | Common:1; Rare:79 | ||||
| chr12:132687294-132687662 | Common:2; Rare:137; Clinvar:11; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132761807-132762154 | Common:3; Rare:119 | ||||
| chr12:132829026-132829220 | Rare:88 | ||||
| chr12:132887546-132887794 | Rare:77 | ||||
| chr12:132956243-132956378 | Common:1; Rare:34 | ||||
| chr12:132986293-132986446 | Rare:35 | ||||
| chr12:133037192-133037582 | Common:5; Rare:87 | ||||
| chr12:133080721-133080941 | Common:1; Rare:69 | ||||
| chr12:133130232-133130627 | Common:7; Rare:123 | ||||
| chr13:19633455-19633783 | Common:1; Rare:126 |