| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:37639572-37639732 | Rare:55 | ||||
| chr22:37639992-37640091 | Rare:17 | ||||
| chr22:37658235-37658831 | Common:6; Rare:189 | ||||
| chr22:37674991-37675264 | Common:1; Rare:62 | ||||
| chr22:37675309-37675695 | Common:3; Rare:103 | ||||
| chr22:37675902-37676354 | Common:3; Rare:90 | ||||
| chr22:37676767-37676875 | Rare:38 | ||||
| chr22:37677007-37677546 | Common:2; Rare:144 | ||||
| chr22:37686203-37686721 | Common:1; Rare:174 | ||||
| chr22:37745809-37746453 | Common:5; Rare:217; Clinvar (benign):1 | ||||
| chr22:37746549-37746648 | Rare:35 | ||||
| chr22:37805087-37805245 | Rare:44 | ||||
| chr22:37807739-37808011 | Common:4; Rare:104 | ||||
| chr22:37843838-37843947 | Common:1; Rare:27 | ||||
| chr22:37844126-37844193 | Rare:24 |