Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:10928535-10928692 | Common:1; Rare:40 | ||||
chr19:10960717-10961059 | Common:3; Rare:135 | ||||
chr19:11018759-11018971 | Common:1; Rare:54; Clinvar (benign):1 | ||||
chr19:11197510-11197622 | Common:1; Rare:30 | ||||
chr19:11435276-11435440 | Rare:43 | ||||
chr19:11446896-11447097 | Common:1; Rare:62 | ||||
chr19:11559201-11559413 | Common:1; Rare:65 | ||||
chr19:12035667-12035742 | Common:1; Rare:33 | ||||
chr19:12441113-12441366 | Common:4; Rare:73 | ||||
chr19:12551421-12551683 | Common:2; Rare:75 | ||||
chr19:12610719-12611021 | Common:1; Rare:101 | ||||
chr19:12666683-12666838 | Rare:63; Clinvar:4 | ||||
chr19:12696619-12696690 | Rare:31 | ||||
chr19:12722514-12722768 | Common:3; Rare:46 | ||||
chr19:12791334-12791509 | Rare:36 |