| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:39319736-39319779 | Rare:11 | ||||
| chr22:39349766-39350056 | Common:1; Rare:88 | ||||
| chr22:39399634-39399836 | Common:3; Rare:87 | ||||
| chr22:39502158-39502415 | Rare:78 | ||||
| chr22:39532666-39533028 | Common:2; Rare:142 | ||||
| chr22:40044109-40044360 | Common:2; Rare:60 | ||||
| chr22:40044528-40044959 | Common:3; Rare:107 | ||||
| chr22:40177756-40178011 | Rare:75 | ||||
| chr22:40346434-40346709 | Common:1; Rare:120; Clinvar:12; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr22:40636649-40637031 | Common:2; Rare:107 | ||||
| chr22:40856562-40857165 | Common:3; Rare:243; Clinvar:4 | ||||
| chr22:40951085-40951475 | Common:2; Rare:121 | ||||
| chr22:40951625-40951837 | Common:2; Rare:56 | ||||
| chr22:41091419-41091842 | Common:6; Rare:155 | ||||
| chr22:41285978-41286046 | Common:1; Rare:19 |