| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:26195090-26195339 | Rare:85; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr2:26244563-26244975 | Common:2; Rare:154; Clinvar:6; Clinvar (benign):9 | ||||
| chr2:26345785-26346184 | Common:1; Rare:120 | ||||
| chr2:26764188-26764330 | Common:1; Rare:56 | ||||
| chr2:27032822-27033004 | Rare:73 | ||||
| chr2:27051539-27051706 | Rare:50 | ||||
| chr2:27071502-27072090 | Common:2; Rare:160 | ||||
| chr2:27078523-27078685 | Common:2; Rare:44 | ||||
| chr2:27086587-27086782 | Rare:55 | ||||
| chr2:27211904-27212125 | Common:3; Rare:80 | ||||
| chr2:27212252-27212386 | Common:2; Rare:68 | ||||
| chr2:27217318-27217501 | Rare:79 | ||||
| chr2:27323007-27323154 | Rare:42; Clinvar (benign):1 | ||||
| chr2:27356750-27357170 | Common:2; Rare:121 | ||||
| chr2:27370277-27370648 | Common:1; Rare:152 |