| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:24555888-24556044 | Rare:48 | ||||
| chr22:26483772-26483880 | Common:4; Rare:45; Clinvar:5; Clinvar (benign):1 | ||||
| chr22:26512428-26512550 | Common:1; Rare:55 | ||||
| chr22:26590077-26590211 | Common:3; Rare:53 | ||||
| chr22:27919177-27919518 | Common:5; Rare:150 | ||||
| chr22:28741791-28742072 | Common:2; Rare:86; Clinvar:1; Clinvar (benign):3 | ||||
| chr22:28742401-28742703 | Common:1; Rare:74 | ||||
| chr22:28800395-28800714 | Common:5; Rare:116 | ||||
| chr22:29267894-29268348 | Common:2; Rare:130 | ||||
| chr22:29767053-29767402 | Common:4; Rare:109 | ||||
| chr22:30289540-30289850 | Common:2; Rare:62 | ||||
| chr22:30356817-30357010 | Common:1; Rare:70 | ||||
| chr22:30396964-30397016 | Common:1; Rare:9 | ||||
| chr22:30591860-30592162 | Common:5; Rare:93 | ||||
| chr22:30607002-30607315 | Common:3; Rare:103; Clinvar:4; Clinvar (benign):3 |