Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:984147-984356 | Common:4; Rare:73 | ||||
chr19:1269036-1269398 | Common:3; Rare:137 | ||||
chr19:1354768-1354996 | Common:2; Rare:95 | ||||
chr19:2328562-2328703 | Common:2; Rare:70 | ||||
chr19:2785275-2785537 | Common:3; Rare:76 | ||||
chr19:3982847-3983194 | Common:5; Rare:126; Clinvar:1; Clinvar (benign):3 | ||||
chr19:4182541-4182659 | Rare:39 | ||||
chr19:4471967-4472307 | Common:4; Rare:118 | ||||
chr19:5293222-5293408 | Common:1; Rare:85 | ||||
chr19:5622699-5623230 | Common:5; Rare:216 | ||||
chr19:5680705-5681019 | Rare:71 | ||||
chr19:5978078-5978373 | Common:3; Rare:110 | ||||
chr19:7395033-7395163 | Common:3; Rare:37 | ||||
chr19:7629539-7629848 | Common:5; Rare:111; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr19:7943656-7943974 | Rare:77 |