| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:43862414-43862650 | Common:7; Rare:93 | ||||
| chr22:43955300-43955571 | Common:3; Rare:82 | ||||
| chr22:44498168-44498481 | Common:2; Rare:119 | ||||
| chr22:45163790-45164008 | Common:2; Rare:79 | ||||
| chr22:45413578-45413716 | Rare:54 | ||||
| chr22:46250268-46250404 | Common:1; Rare:43 | ||||
| chr22:46296732-46296925 | Common:1; Rare:65 | ||||
| chr22:46335621-46335770 | Common:2; Rare:63; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr22:46762496-46762669 | Common:3; Rare:64 | ||||
| chr22:50244986-50245114 | Common:1; Rare:52 | ||||
| chr22:50562887-50563011 | Common:3; Rare:37 | ||||
| chr22:50582784-50583120 | Common:7; Rare:103; Clinvar:2; Clinvar (benign):3 | ||||
| chr22:50783628-50783842 | Common:1; Rare:63 | ||||
| chr3:1092777-1093049 | Common:1; Rare:83 | ||||
| chr3:3126707-3126990 | Common:7; Rare:127; Clinvar (benign):2 |