| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:23767905-23768016 | Rare:30 | ||||
| chr22:23838992-23839225 | Rare:78 | ||||
| chr22:23857662-23857918 | Common:2; Rare:90 | ||||
| chr22:23894205-23894548 | Common:3; Rare:125 | ||||
| chr22:23894576-23894943 | Common:3; Rare:151; Clinvar:1 | ||||
| chr22:24011656-24011757 | Common:2; Rare:22 | ||||
| chr22:24245071-24245272 | Common:2; Rare:35 | ||||
| chr22:24270602-24270982 | Common:4; Rare:128 | ||||
| chr22:24271080-24271190 | Common:1; Rare:53 | ||||
| chr22:24304098-24304383 | Common:1; Rare:50 | ||||
| chr22:24554981-24555430 | Common:4; Rare:160 | ||||
| chr22:24555884-24556065 | Rare:53 | ||||
| chr22:24952616-24952770 | Rare:48 | ||||
| chr22:26483752-26483880 | Common:4; Rare:57; Clinvar:5; Clinvar (benign):1 | ||||
| chr22:26512447-26512550 | Common:1; Rare:48 |