| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:42720817-42720983 | Common:1; Rare:50 | ||||
| chr22:42857187-42857484 | Common:3; Rare:121 | ||||
| chr22:43015099-43015384 | Common:2; Rare:117 | ||||
| chr22:43955275-43955571 | Common:3; Rare:90 | ||||
| chr22:44498201-44498479 | Common:2; Rare:113 | ||||
| chr22:45163694-45164034 | Common:5; Rare:126 | ||||
| chr22:45309721-45309936 | Common:1; Rare:83 | ||||
| chr22:46053665-46053879 | Rare:72 | ||||
| chr22:46250268-46250432 | Common:2; Rare:56 | ||||
| chr22:46267840-46268032 | Common:1; Rare:58 | ||||
| chr22:46296710-46296922 | Common:2; Rare:78 | ||||
| chr22:46335599-46335819 | Common:5; Rare:104; Clinvar:11; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr22:46762496-46762690 | Common:3; Rare:73 | ||||
| chr22:49853603-49853925 | Common:2; Rare:115 | ||||
| chr22:50582818-50583142 | Common:5; Rare:99; Clinvar:2; Clinvar (benign):1 |