| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:17638677-17638843 | Rare:60 | ||||
| chr22:17774395-17774587 | Rare:67 | ||||
| chr22:18077800-18078028 | Common:5; Rare:73; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:19178462-19178522 | Common:1; Rare:14 | ||||
| chr22:19432378-19432595 | Common:2; Rare:88 | ||||
| chr22:19447677-19447767 | Common:1; Rare:45 | ||||
| chr22:19479687-19479949 | Common:4; Rare:66 | ||||
| chr22:19854835-19855023 | Rare:73 | ||||
| chr22:19941759-19941886 | Rare:52; Clinvar:3 | ||||
| chr22:20020892-20021151 | Common:1; Rare:87 | ||||
| chr22:20080086-20080293 | Rare:74 | ||||
| chr22:20117257-20117571 | Common:2; Rare:97 | ||||
| chr22:20320009-20320158 | Common:1; Rare:50 | ||||
| chr22:20495787-20496007 | Common:2; Rare:79 | ||||
| chr22:20507547-20507622 | Rare:20 |