| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50526412-50526610 | Common:2; Rare:99; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr22:50526886-50527185 | Rare:102; Clinvar (pathogenic):1 | ||||
| chr22:50529991-50530247 | Common:1; Rare:70; Clinvar:1 | ||||
| chr22:50530339-50530492 | Common:1; Rare:55 | ||||
| chr22:50530521-50530577 | Rare:18 | ||||
| chr22:50530935-50531140 | Rare:65 | ||||
| chr22:50531144-50531297 | Common:1; Rare:56 | ||||
| chr22:50531564-50531893 | Common:3; Rare:77 | ||||
| chr22:50532450-50532605 | Common:1; Rare:34 | ||||
| chr22:50562768-50563150 | Common:6; Rare:100 | ||||
| chr22:50582173-50582312 | Common:1; Rare:49; Clinvar:1; Clinvar (benign):2 | ||||
| chr22:50582606-50582868 | Common:5; Rare:111; Clinvar:3; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr22:50582921-50583230 | Common:4; Rare:99 | ||||
| chr22:50583353-50583374 | Rare:6 | ||||
| chr22:50628019-50628413 | Common:9; Rare:158; Clinvar:3; Clinvar (benign):1 |