| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41092107-41092449 | Common:3; Rare:129 | ||||
| chr22:41286175-41286424 | Common:2; Rare:74 | ||||
| chr22:41446506-41446582 | Rare:14 | ||||
| chr22:41446683-41446979 | Common:1; Rare:112 | ||||
| chr22:41469002-41469386 | Common:1; Rare:140 | ||||
| chr22:41589764-41589893 | Common:1; Rare:60 | ||||
| chr22:41621005-41621364 | Common:7; Rare:133 | ||||
| chr22:41800528-41800688 | Common:1; Rare:50 | ||||
| chr22:41832909-41833231 | Common:3; Rare:110 | ||||
| chr22:41899063-41899288 | Common:2; Rare:49 | ||||
| chr22:42070782-42070991 | Common:3; Rare:43 | ||||
| chr22:42079497-42079823 | Common:2; Rare:95 | ||||
| chr22:42090607-42091138 | Common:2; Rare:204; Clinvar (pathogenic):1 | ||||
| chr22:42130859-42130905 | Rare:12 | ||||
| chr22:42614856-42615251 | Common:3; Rare:166 |