| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41469062-41469142 | Rare:30 | ||||
| chr22:41544444-41544718 | Common:3; Rare:80 | ||||
| chr22:41620978-41621370 | Common:7; Rare:140 | ||||
| chr22:41800506-41800702 | Common:1; Rare:61 | ||||
| chr22:41832909-41833149 | Common:3; Rare:80 | ||||
| chr22:41946708-41946994 | Common:3; Rare:80 | ||||
| chr22:41947093-41947204 | Rare:41 | ||||
| chr22:42070802-42070916 | Common:1; Rare:25 | ||||
| chr22:42090668-42090956 | Common:2; Rare:129; Clinvar (pathogenic):1 | ||||
| chr22:42519790-42519887 | Common:1; Rare:41 | ||||
| chr22:42614858-42615246 | Common:3; Rare:161 | ||||
| chr22:42649333-42649615 | Common:6; Rare:96 | ||||
| chr22:42857178-42857431 | Common:3; Rare:106 | ||||
| chr22:43015099-43015384 | Common:2; Rare:117 | ||||
| chr22:43812208-43812441 | Common:3; Rare:78 |