| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:41915031-41915337 | Common:7; Rare:66 | ||||
| chr22:41926705-41927093 | Common:3; Rare:100; Clinvar:1; Clinvar (benign):2 | ||||
| chr22:41940198-41940243 | Common:1; Rare:9 | ||||
| chr22:41946631-41946971 | Common:3; Rare:81 | ||||
| chr22:41947046-41947258 | Common:1; Rare:72 | ||||
| chr22:41998574-41998848 | Common:3; Rare:104 | ||||
| chr22:42070332-42070376 | Rare:15; Clinvar:1 | ||||
| chr22:42070496-42071106 | Common:5; Rare:136; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:42074487-42074660 | Common:3; Rare:43 | ||||
| chr22:42079359-42079770 | Common:4; Rare:98 | ||||
| chr22:42079881-42080185 | Rare:98 | ||||
| chr22:42090311-42090435 | Common:1; Rare:33 | ||||
| chr22:42090674-42091201 | Common:3; Rare:197; Clinvar (pathogenic):1 | ||||
| chr22:42432357-42432424 | Rare:23 | ||||
| chr22:42519727-42519965 | Common:1; Rare:96 |