| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:37953597-37953738 | Rare:61 | ||||
| chr22:38084145-38084342 | Common:1; Rare:47 | ||||
| chr22:38656391-38656687 | Common:1; Rare:65 | ||||
| chr22:38681810-38681979 | Common:1; Rare:70 | ||||
| chr22:39319601-39319918 | Common:4; Rare:115 | ||||
| chr22:40346458-40346551 | Rare:39; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:40856437-40856746 | Rare:137 | ||||
| chr22:40856806-40857154 | Common:2; Rare:132; Clinvar:3 | ||||
| chr22:41286175-41286458 | Common:2; Rare:81 | ||||
| chr22:41301307-41301610 | Common:1; Rare:85 | ||||
| chr22:41446790-41446956 | Rare:65 | ||||
| chr22:41468997-41469157 | Rare:54 | ||||
| chr22:41621021-41621370 | Common:7; Rare:130 | ||||
| chr22:41800506-41800631 | Rare:40 | ||||
| chr22:41832831-41833139 | Common:3; Rare:97 |