| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:25184270-25184840 | Rare:87 | ||||
| chr2:25311000-25311330 | Rare:53 | ||||
| chr2:25362022-25362328 | Common:4; Rare:68 | ||||
| chr2:25376700-25377110 | Common:4; Rare:108 | ||||
| chr2:25671691-25671938 | Rare:35 | ||||
| chr2:25719614-25720014 | Common:5; Rare:87 | ||||
| chr2:25877280-25877840 | Common:4; Rare:181 | ||||
| chr2:26012193-26012471 | Rare:61 | ||||
| chr2:26012526-26012781 | Common:4; Rare:49 | ||||
| chr2:26018060-26018558 | Common:5; Rare:140 | ||||
| chr2:26033212-26033480 | Common:2; Rare:96 | ||||
| chr2:26035040-26035733 | Common:3; Rare:253 | ||||
| chr2:26178868-26178990 | Common:6; Rare:36 | ||||
| chr2:26299640-26300213 | Common:17; Rare:248 | ||||
| chr2:26503380-26503990 | Common:4; Rare:186; Clinvar:3; Clinvar (benign):1 |