Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:4792603-4793024 | Common:2; Rare:263 | ||||
chr19:4812760-4813050 | Common:2; Rare:54 | ||||
chr19:4851756-4852500 | Common:11; Rare:290 | ||||
chr19:4929000-4929400 | Common:8; Rare:205 | ||||
chr19:5804820-5805130 | Common:4; Rare:152 | ||||
chr19:5880480-5880930 | Rare:173 | ||||
chr19:5961950-5962370 | Common:3; Rare:134 | ||||
chr19:6413944-6414258 | Rare:124 | ||||
chr19:6707240-6707550 | Common:2; Rare:95; Clinvar (benign):2 | ||||
chr19:6707710-6708561 | Common:5; Rare:341; Clinvar:2; Clinvar (benign):6 | ||||
chr19:6712196-6712719 | Common:1; Rare:283; Clinvar:3; Clinvar (benign):7 | ||||
chr19:6717490-6717790 | Common:13; Rare:121 | ||||
chr19:6718000-6718300 | Common:2; Rare:84; Clinvar:2 | ||||
chr19:6719170-6719700 | Common:5; Rare:196; Clinvar (pathogenic):2 | ||||
chr19:6723101-6723462 | Common:5; Rare:112 |