| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:37953550-37953771 | Rare:89 | ||||
| chr22:38201786-38202093 | Common:2; Rare:87 | ||||
| chr22:38467937-38468112 | Common:1; Rare:54 | ||||
| chr22:38506264-38506686 | Common:1; Rare:139 | ||||
| chr22:38656389-38656706 | Common:1; Rare:71 | ||||
| chr22:38681817-38682239 | Common:3; Rare:160 | ||||
| chr22:38794094-38794344 | Rare:68 | ||||
| chr22:38872190-38872452 | Rare:70 | ||||
| chr22:39319538-39319841 | Common:3; Rare:134 | ||||
| chr22:39502147-39502412 | Rare:79 | ||||
| chr22:40044528-40044875 | Common:2; Rare:81 | ||||
| chr22:40177793-40177950 | Rare:44 | ||||
| chr22:40346409-40346578 | Common:1; Rare:76; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr22:40636668-40637022 | Common:2; Rare:98 | ||||
| chr22:40819283-40819518 | Common:11; Rare:110 |