| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20917781-20918015 | Rare:80 | ||||
| chr22:20981854-20982082 | Common:2; Rare:61; Clinvar (benign):1 | ||||
| chr22:20982110-20982480 | Common:2; Rare:110; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr22:21001569-21001768 | Common:1; Rare:58 | ||||
| chr22:21001778-21001958 | Common:1; Rare:70 | ||||
| chr22:21001992-21002314 | Common:7; Rare:126 | ||||
| chr22:21567602-21567836 | Common:2; Rare:83 | ||||
| chr22:21629354-21629620 | Common:2; Rare:79 | ||||
| chr22:21629922-21630202 | Common:2; Rare:107 | ||||
| chr22:21641970-21642408 | Common:2; Rare:133 | ||||
| chr22:21651875-21652267 | Common:2; Rare:83 | ||||
| chr22:21665885-21666070 | Rare:55 | ||||
| chr22:21666185-21666427 | Common:1; Rare:69 | ||||
| chr22:21735786-21735938 | Rare:45 | ||||
| chr22:21866909-21867225 | Common:1; Rare:88 |