| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20079921-20080253 | Common:1; Rare:107 | ||||
| chr22:20117183-20117566 | Common:3; Rare:121 | ||||
| chr22:20319994-20320158 | Common:2; Rare:53 | ||||
| chr22:20495771-20495919 | Common:1; Rare:55 | ||||
| chr22:20858718-20859105 | Common:6; Rare:197; Clinvar:3; Clinvar (benign):4 | ||||
| chr22:20982201-20982353 | Common:2; Rare:34; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:21002042-21002215 | Common:3; Rare:70 | ||||
| chr22:21642055-21642348 | Common:2; Rare:89 | ||||
| chr22:21938234-21938300 | Rare:29 | ||||
| chr22:22508724-22508913 | Rare:55 | ||||
| chr22:23786872-23787032 | Common:1; Rare:60; Clinvar:3 | ||||
| chr22:23857617-23857910 | Common:2; Rare:104 | ||||
| chr22:24555881-24556066 | Rare:54 | ||||
| chr22:26483757-26484015 | Common:6; Rare:111; Clinvar:5; Clinvar (benign):1 | ||||
| chr22:26512432-26512560 | Common:1; Rare:58 |