| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:40346445-40346664 | Rare:101; Clinvar:10; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr22:40636661-40637012 | Common:2; Rare:96 | ||||
| chr22:40856431-40856742 | Rare:139 | ||||
| chr22:40856957-40857154 | Rare:86; Clinvar:3 | ||||
| chr22:41286142-41286428 | Common:2; Rare:92 | ||||
| chr22:41468633-41468747 | Common:2; Rare:35 | ||||
| chr22:41620992-41621384 | Common:7; Rare:141 | ||||
| chr22:41800489-41800688 | Common:1; Rare:68 | ||||
| chr22:41832798-41833194 | Common:3; Rare:125 | ||||
| chr22:42070761-42070971 | Common:2; Rare:46 | ||||
| chr22:42090732-42090945 | Common:1; Rare:78; Clinvar (pathogenic):1 | ||||
| chr22:42614840-42615246 | Common:3; Rare:171 | ||||
| chr22:42649311-42649482 | Common:1; Rare:67 | ||||
| chr22:43089321-43089490 | Common:3; Rare:58 | ||||
| chr22:43955303-43955566 | Common:3; Rare:80 |