| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:42649311-42649482 | Common:1; Rare:67 | ||||
| chr22:42857178-42857430 | Common:3; Rare:105 | ||||
| chr22:43015075-43015384 | Common:2; Rare:127 | ||||
| chr22:43089305-43089480 | Common:4; Rare:64 | ||||
| chr22:43812191-43812434 | Common:3; Rare:79 | ||||
| chr22:43955303-43955556 | Common:3; Rare:75 | ||||
| chr22:44024159-44024342 | Common:1; Rare:63 | ||||
| chr22:45163758-45164015 | Common:2; Rare:97 | ||||
| chr22:45212359-45212685 | Common:3; Rare:90 | ||||
| chr22:45413578-45413753 | Common:1; Rare:71 | ||||
| chr22:46250261-46250408 | Common:2; Rare:45 | ||||
| chr22:46267808-46268046 | Common:1; Rare:71 | ||||
| chr22:46296711-46296922 | Common:2; Rare:77 | ||||
| chr22:46335614-46335809 | Common:5; Rare:93; Clinvar:8; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr22:46762455-46762676 | Common:3; Rare:83 |