| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20394060-20394174 | Rare:27 | ||||
| chr22:20495781-20495913 | Common:1; Rare:50 | ||||
| chr22:20507485-20507624 | Rare:35 | ||||
| chr22:20858809-20859093 | Common:4; Rare:141; Clinvar:3; Clinvar (benign):3 | ||||
| chr22:20982196-20982353 | Common:2; Rare:36; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:21002071-21002223 | Common:3; Rare:56 | ||||
| chr22:21642042-21642366 | Common:2; Rare:100 | ||||
| chr22:21867412-21867564 | Common:1; Rare:34 | ||||
| chr22:23145192-23145507 | Common:2; Rare:105 | ||||
| chr22:24245080-24245272 | Common:2; Rare:32 | ||||
| chr22:24555025-24555428 | Common:4; Rare:142 | ||||
| chr22:24555878-24556045 | Rare:52 | ||||
| chr22:26483764-26483949 | Common:4; Rare:71; Clinvar:5; Clinvar (benign):1 | ||||
| chr22:26512428-26512550 | Common:1; Rare:55 | ||||
| chr22:27919188-27919510 | Common:5; Rare:142 |