| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:17638689-17638827 | Rare:50 | ||||
| chr22:17841977-17842162 | Rare:53 | ||||
| chr22:18077829-18078098 | Common:5; Rare:89; Clinvar:3; Clinvar (benign):3 | ||||
| chr22:18149829-18150134 | Common:2; Rare:72 | ||||
| chr22:19291707-19291887 | Common:8; Rare:54 | ||||
| chr22:19432284-19432610 | Common:4; Rare:140 | ||||
| chr22:19447677-19447786 | Common:1; Rare:52 | ||||
| chr22:19478929-19479060 | Common:1; Rare:44 | ||||
| chr22:19479112-19479466 | Common:4; Rare:127 | ||||
| chr22:19479693-19479956 | Common:4; Rare:70 | ||||
| chr22:19854806-19855023 | Rare:84 | ||||
| chr22:19941602-19941881 | Common:1; Rare:111; Clinvar:6; Clinvar (benign):7 | ||||
| chr22:19963042-19963276 | Common:1; Rare:58 | ||||
| chr22:20020891-20021151 | Common:1; Rare:88 | ||||
| chr22:20079964-20080300 | Common:1; Rare:115 |