Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:29767468-29767596 | Common:1; Rare:53 | ||||
chr22:30356871-30356989 | Common:1; Rare:37 | ||||
chr22:30607056-30607288 | Common:3; Rare:73; Clinvar:3; Clinvar (benign):3 | ||||
chr22:31160092-31160201 | Common:1; Rare:38 | ||||
chr22:35399915-35400174 | Rare:89 | ||||
chr22:37019416-37019848 | Common:5; Rare:127 | ||||
chr22:37560352-37560538 | Rare:64 | ||||
chr22:37849301-37849446 | Rare:87 | ||||
chr22:37953609-37953737 | Rare:53 | ||||
chr22:38656337-38656746 | Common:1; Rare:109 | ||||
chr22:38681821-38682030 | Common:2; Rare:88 | ||||
chr22:38700919-38701004 | Rare:34 | ||||
chr22:40346462-40346577 | Rare:54; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr22:41286142-41286379 | Common:2; Rare:74 | ||||
chr22:41301412-41301621 | Rare:65 |