| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:39319601-39319804 | Common:3; Rare:88 | ||||
| chr22:39502155-39502371 | Rare:59 | ||||
| chr22:40044528-40044870 | Common:2; Rare:80 | ||||
| chr22:40346434-40346556 | Rare:52; Clinvar:2; Clinvar (benign):2 | ||||
| chr22:40856590-40856706 | Rare:50 | ||||
| chr22:40856957-40857159 | Rare:90; Clinvar:3 | ||||
| chr22:41286158-41286516 | Common:2; Rare:113 | ||||
| chr22:41301326-41301610 | Common:1; Rare:81 | ||||
| chr22:41446784-41446966 | Rare:75 | ||||
| chr22:41468635-41468800 | Common:2; Rare:44 | ||||
| chr22:41469063-41469144 | Rare:32 | ||||
| chr22:41621005-41621370 | Common:7; Rare:135 | ||||
| chr22:41832876-41833137 | Common:3; Rare:83 | ||||
| chr22:42070770-42071003 | Common:3; Rare:51 | ||||
| chr22:42090707-42090944 | Common:2; Rare:100; Clinvar (pathogenic):1 |