| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:23974368-23974690 | Common:1; Rare:4 | ||||
| chr22:24011035-24011462 | Common:43; Rare:215 | ||||
| chr22:24011674-24011757 | Common:1; Rare:18 | ||||
| chr22:24270684-24270962 | Common:3; Rare:100 | ||||
| chr22:24271046-24271203 | Common:2; Rare:66 | ||||
| chr22:24555877-24556065 | Rare:55 | ||||
| chr22:24952597-24952753 | Rare:46 | ||||
| chr22:25564785-25565013 | Common:1; Rare:96 | ||||
| chr22:26169327-26169756 | Common:2; Rare:114 | ||||
| chr22:26429145-26429467 | Common:3; Rare:112 | ||||
| chr22:26483740-26483967 | Common:4; Rare:96; Clinvar:6; Clinvar (benign):1 | ||||
| chr22:26512413-26512567 | Common:2; Rare:65 | ||||
| chr22:27801068-27801253 | Common:1; Rare:42 | ||||
| chr22:27919190-27919545 | Common:5; Rare:159 | ||||
| chr22:28741800-28742078 | Common:2; Rare:82; Clinvar:1; Clinvar (benign):1 |