| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41947089-41947214 | Rare:44 | ||||
| chr22:42070782-42070942 | Common:1; Rare:31 | ||||
| chr22:42079491-42079763 | Common:2; Rare:71 | ||||
| chr22:42090730-42090945 | Common:1; Rare:79; Clinvar (pathogenic):1 | ||||
| chr22:42614858-42615246 | Common:3; Rare:161 | ||||
| chr22:42649322-42649483 | Common:1; Rare:65 | ||||
| chr22:43015104-43015386 | Common:2; Rare:118 | ||||
| chr22:43151471-43151598 | Common:1; Rare:30 | ||||
| chr22:43955303-43955556 | Common:3; Rare:75 | ||||
| chr22:45163674-45164021 | Common:4; Rare:127 | ||||
| chr22:45671986-45672108 | Rare:61 | ||||
| chr22:46053778-46053901 | Rare:43 | ||||
| chr22:46250268-46250403 | Common:1; Rare:42 | ||||
| chr22:46267878-46268030 | Common:1; Rare:46 | ||||
| chr22:46296711-46296918 | Common:2; Rare:75 |