Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:9827810-9827948 | Common:1; Rare:52 | ||||
chr19:10333517-10333709 | Rare:64 | ||||
chr19:10403403-10403834 | Rare:144 | ||||
chr19:10502713-10502919 | Rare:54 | ||||
chr19:10568968-10569223 | Common:2; Rare:67 | ||||
chr19:10701387-10701463 | Rare:27 | ||||
chr19:10960708-10961164 | Common:3; Rare:165; Clinvar (benign):2 | ||||
chr19:11089315-11089473 | Rare:25; Clinvar:8; Clinvar (pathogenic):1 | ||||
chr19:11197510-11197610 | Rare:25 | ||||
chr19:11435148-11435442 | Common:2; Rare:76 | ||||
chr19:11559210-11559314 | Common:1; Rare:38 | ||||
chr19:11848642-11848773 | Common:1; Rare:36 | ||||
chr19:11887671-11887829 | Common:1; Rare:49 | ||||
chr19:11924961-11925134 | Common:6; Rare:48 | ||||
chr19:12035647-12035773 | Common:1; Rare:50 |