| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:20501305-20501536 | Common:19; Rare:100 | ||||
| chr2:26969108-26969418 | Common:3; Rare:53 | ||||
| chr2:28391706-28391825 | Rare:29 | ||||
| chr2:28393359-28393688 | Common:1; Rare:97 | ||||
| chr2:28584380-28584484 | Common:2; Rare:22 | ||||
| chr2:33210681-33210951 | Common:2; Rare:59 | ||||
| chr2:33212170-33212431 | Common:1; Rare:58 | ||||
| chr2:33214407-33214645 | Common:1; Rare:48 | ||||
| chr2:38076921-38077179 | Common:1; Rare:70 | ||||
| chr2:38146985-38147222 | Common:1; Rare:59 | ||||
| chr2:39737763-39738001 | Common:1; Rare:53 | ||||
| chr2:47790716-47791036 | Common:2; Rare:84; Clinvar:15; Clinvar (benign):13; Clinvar (pathogenic):1 | ||||
| chr2:47906488-47906815 | Common:2; Rare:114 | ||||
| chr2:53971856-53972092 | Common:2; Rare:65 | ||||
| chr2:54634742-54634954 | Common:2; Rare:46 |