| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:17638696-17638829 | Rare:48 | ||||
| chr22:17774406-17774542 | Rare:48 | ||||
| chr22:18077829-18078047 | Common:4; Rare:72; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:18149817-18150188 | Common:2; Rare:86 | ||||
| chr22:19144627-19144831 | Common:3; Rare:75 | ||||
| chr22:19178430-19178519 | Common:1; Rare:25 | ||||
| chr22:19291696-19291932 | Common:10; Rare:70 | ||||
| chr22:19432302-19432606 | Common:4; Rare:130 | ||||
| chr22:19447677-19447734 | Rare:38 | ||||
| chr22:19479112-19479466 | Common:4; Rare:127 | ||||
| chr22:19525296-19525542 | Common:1; Rare:50 | ||||
| chr22:19854791-19855106 | Common:1; Rare:119 | ||||
| chr22:19941477-19942119 | Common:4; Rare:178; Clinvar:7; Clinvar (benign):7 | ||||
| chr22:19987173-19987461 | Common:2; Rare:115 | ||||
| chr22:20079936-20080302 | Common:1; Rare:122 |