| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50314485-50314628 | Common:1; Rare:68 | ||||
| chr22:50405859-50406097 | Rare:15 | ||||
| chr22:50437292-50437581 | Common:2; Rare:88 | ||||
| chr22:50448609-50448691 | Rare:22 | ||||
| chr22:50459362-50459580 | Common:2; Rare:88 | ||||
| chr22:50460641-50460875 | Common:1; Rare:91; Clinvar (benign):1 | ||||
| chr22:50462578-50462829 | Common:3; Rare:94 | ||||
| chr22:50465001-50465240 | Common:1; Rare:97; Clinvar (pathogenic):1 | ||||
| chr22:50466180-50466417 | Rare:85 | ||||
| chr22:50466433-50466569 | Rare:52 | ||||
| chr3:3133231-3133497 | Common:6; Rare:64 | ||||
| chr3:3135097-3135279 | Common:2; Rare:39 | ||||
| chr3:3141133-3141160 | Rare:5 | ||||
| chr3:3152582-3152662 | Common:1; Rare:26 | ||||
| chr3:4811110-4811304 | Rare:44 |