| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20507490-20507647 | Rare:48 | ||||
| chr22:20858731-20859121 | Common:7; Rare:197; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr22:20982196-20982353 | Common:2; Rare:36; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:21002102-21002215 | Common:3; Rare:41 | ||||
| chr22:23750947-23751198 | Common:3; Rare:85 | ||||
| chr22:23894210-23894499 | Common:3; Rare:103 | ||||
| chr22:23894575-23894823 | Common:3; Rare:94 | ||||
| chr22:24244609-24244656 | Rare:19 | ||||
| chr22:24245064-24245271 | Common:2; Rare:37 | ||||
| chr22:24270933-24270962 | Rare:3 | ||||
| chr22:24555889-24556055 | Rare:50 | ||||
| chr22:26483752-26483964 | Common:4; Rare:91; Clinvar:5; Clinvar (benign):1 | ||||
| chr22:26512428-26512552 | Common:1; Rare:55 | ||||
| chr22:26590077-26590220 | Common:3; Rare:58 | ||||
| chr22:27919195-27919518 | Common:5; Rare:144 |