| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20020899-20021164 | Common:1; Rare:90 | ||||
| chr22:20079930-20080275 | Common:1; Rare:112 | ||||
| chr22:20117175-20117586 | Common:3; Rare:134 | ||||
| chr22:20319994-20320348 | Common:2; Rare:105 | ||||
| chr22:20495768-20495984 | Common:2; Rare:80 | ||||
| chr22:20507452-20507627 | Rare:46 | ||||
| chr22:20858709-20859115 | Common:8; Rare:205; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr22:20917286-20917461 | Rare:70 | ||||
| chr22:20982201-20982353 | Common:2; Rare:34; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:21002094-21002273 | Common:5; Rare:65 | ||||
| chr22:21642062-21642348 | Common:2; Rare:86 | ||||
| chr22:21938144-21938374 | Rare:70 | ||||
| chr22:23894200-23894544 | Common:4; Rare:125 | ||||
| chr22:23974356-23974684 | Common:1; Rare:3 | ||||
| chr22:24245058-24245228 | Rare:28 |