Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:45091591-45091792 | Common:1; Rare:52 | ||||
chr19:45406339-45406649 | Common:1; Rare:68 | ||||
chr19:45507228-45507516 | Common:1; Rare:74 | ||||
chr19:45768251-45768329 | Rare:34; Clinvar (benign):1 | ||||
chr19:45769192-45769378 | Rare:63 | ||||
chr19:45864147-45864331 | Common:2; Rare:44 | ||||
chr19:45902611-45902913 | Common:3; Rare:85 | ||||
chr19:46296786-46297057 | Common:4; Rare:100 | ||||
chr19:46298111-46298443 | Common:5; Rare:77 | ||||
chr19:46346941-46347105 | Common:3; Rare:52 | ||||
chr19:46413521-46413884 | Common:1; Rare:105 | ||||
chr19:46600908-46600975 | Common:1; Rare:24 | ||||
chr19:46600984-46601409 | Common:4; Rare:147; Clinvar (benign):1 | ||||
chr19:46745971-46746061 | Common:3; Rare:24 | ||||
chr19:47112166-47112340 | Rare:55 |