Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:44961428-44961482 | Rare:15 | ||||
chr19:45075364-45075697 | Common:1; Rare:70 | ||||
chr19:45717264-45717497 | Common:1; Rare:75 | ||||
chr19:47244248-47244443 | Common:1; Rare:42 | ||||
chr19:47600337-47600620 | Rare:69 | ||||
chr19:49200455-49200644 | Common:3; Rare:72; Clinvar:1; Clinvar (benign):1 | ||||
chr19:49403287-49403546 | Common:6; Rare:64 | ||||
chr19:49403640-49403941 | Common:2; Rare:62 | ||||
chr19:49823512-49823762 | Common:3; Rare:55 | ||||
chr19:49924358-49924604 | Common:4; Rare:63 | ||||
chr19:50419653-50419851 | Common:1; Rare:51 | ||||
chr19:51394233-51394558 | Common:4; Rare:71 | ||||
chr19:52942539-52942789 | Common:8; Rare:91 | ||||
chr19:53196902-53197120 | Common:9; Rare:42 | ||||
chr19:55006086-55006234 | Common:3; Rare:67 |