| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:20446854-20447109 | Common:6; Rare:213 | ||||
| chr2:20651044-20651287 | Rare:143 | ||||
| chr2:20666341-20666741 | Common:1; Rare:143 | ||||
| chr2:20666867-20667200 | Common:14; Rare:122 | ||||
| chr2:20823032-20823198 | Common:2; Rare:111 | ||||
| chr2:21043498-21043740 | Common:1; Rare:61; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:21043784-21044318 | Common:9; Rare:253; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:21123820-21124006 | Common:2; Rare:121 | ||||
| chr2:23927050-23927339 | Common:6; Rare:193 | ||||
| chr2:23940365-23940540 | Common:6; Rare:124 | ||||
| chr2:24047320-24047617 | Common:2; Rare:140 | ||||
| chr2:24049570-24049794 | Common:2; Rare:119 | ||||
| chr2:24076202-24076549 | Rare:157 | ||||
| chr2:24084770-24085250 | Common:6; Rare:95 | ||||
| chr2:24122990-24123510 | Common:3; Rare:173 |