| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:46915733-46915944 | Common:2; Rare:69; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:47176424-47176861 | Common:4; Rare:197; Clinvar (benign):5 | ||||
| chr2:47345045-47345148 | Rare:26 | ||||
| chr2:47369245-47369556 | Common:4; Rare:134; Clinvar:11; Clinvar (benign):5 | ||||
| chr2:47905507-47905696 | Common:3; Rare:99 | ||||
| chr2:48440631-48440823 | Common:5; Rare:86 | ||||
| chr2:53767559-53767858 | Common:4; Rare:103 | ||||
| chr2:53786842-53787169 | Common:1; Rare:122 | ||||
| chr2:53970780-53971173 | Common:12; Rare:143 | ||||
| chr2:54330747-54330941 | Common:3; Rare:73 | ||||
| chr2:55050287-55050419 | Common:1; Rare:51 | ||||
| chr2:55050441-55050730 | Common:4; Rare:85 | ||||
| chr2:55232245-55232719 | Common:3; Rare:131 | ||||
| chr2:55269205-55269324 | Common:2; Rare:34 | ||||
| chr2:55519452-55519794 | Common:1; Rare:103 |