| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:38656391-38656706 | Common:1; Rare:70 | ||||
| chr22:38681792-38682020 | Common:2; Rare:99 | ||||
| chr22:38794088-38794338 | Common:1; Rare:64 | ||||
| chr22:38872185-38872431 | Rare:66 | ||||
| chr22:39040829-39040891 | Common:1; Rare:15 | ||||
| chr22:39319594-39319838 | Common:3; Rare:100 | ||||
| chr22:39502158-39502408 | Rare:73 | ||||
| chr22:39532680-39532866 | Common:2; Rare:85 | ||||
| chr22:40044140-40044341 | Common:2; Rare:45 | ||||
| chr22:40044525-40044874 | Common:2; Rare:83 | ||||
| chr22:40177787-40177966 | Rare:58 | ||||
| chr22:40346425-40346684 | Common:1; Rare:114; Clinvar:12; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr22:40533743-40533941 | Rare:43 | ||||
| chr22:40636668-40637033 | Common:2; Rare:102 | ||||
| chr22:40819311-40819553 | Common:11; Rare:114 |