Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:48469093-48469393 | Common:3; Rare:85 | ||||
chr19:48619139-48619433 | Rare:95 | ||||
chr19:48872226-48872421 | Common:2; Rare:59 | ||||
chr19:48993296-48993912 | Common:7; Rare:202; Clinvar:1; Clinvar (benign):1 | ||||
chr19:49085130-49085492 | Common:3; Rare:145 | ||||
chr19:49527702-49528031 | Common:4; Rare:95 | ||||
chr19:49580527-49580733 | Common:1; Rare:60 | ||||
chr19:49665761-49666029 | Common:3; Rare:132; Clinvar (pathogenic):1 | ||||
chr19:49877343-49877694 | Common:1; Rare:84 | ||||
chr19:49929377-49929567 | Common:4; Rare:65 | ||||
chr19:50025347-50025702 | Common:6; Rare:107 | ||||
chr19:50476409-50476541 | Rare:59 | ||||
chr19:51366335-51366595 | Common:8; Rare:73; Clinvar (benign):2 | ||||
chr19:52028336-52028389 | Common:1; Rare:15 | ||||
chr19:52369817-52369950 | Common:1; Rare:45 |