| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:23787257-23787488 | Common:7; Rare:107; Clinvar (benign):2 | ||||
| chr22:23857645-23857930 | Common:5; Rare:194 | ||||
| chr22:23894067-23894576 | Common:8; Rare:231 | ||||
| chr22:23894500-23894941 | Common:6; Rare:298; Clinvar:2 | ||||
| chr22:24011049-24011501 | Common:84; Rare:431 | ||||
| chr22:24270602-24270968 | Common:7; Rare:225 | ||||
| chr22:24271010-24271215 | Common:4; Rare:142 | ||||
| chr22:24555030-24555487 | Common:7; Rare:315 | ||||
| chr22:24555617-24556069 | Rare:205 | ||||
| chr22:24952625-24952772 | Rare:47 | ||||
| chr22:25405348-25405467 | Common:5; Rare:51 | ||||
| chr22:26483712-26483935 | Common:9; Rare:158; Clinvar:11; Clinvar (benign):3 | ||||
| chr22:26512425-26512555 | Common:2; Rare:109 | ||||
| chr22:26590081-26590260 | Common:3; Rare:74 | ||||
| chr22:27801709-27801852 | Common:2; Rare:59 |