Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:73058303-73058634 | Common:3; Rare:101 | ||||
chr14:73136283-73136534 | Common:4; Rare:79; Clinvar:3; Clinvar (benign):1 | ||||
chr14:73458520-73458870 | Common:5; Rare:91 | ||||
chr14:73567902-73568128 | Common:1; Rare:61 | ||||
chr14:73569031-73569299 | Rare:59 | ||||
chr14:73714353-73714447 | Common:1; Rare:38 | ||||
chr14:73851774-73851983 | Common:4; Rare:71 | ||||
chr14:73950066-73950323 | Common:6; Rare:104; Clinvar (benign):4 | ||||
chr14:74019252-74019438 | Common:1; Rare:73 | ||||
chr14:74084397-74084786 | Common:7; Rare:96 | ||||
chr14:74493270-74493777 | Common:4; Rare:160; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr14:74713058-74713232 | Rare:94 | ||||
chr14:74763136-74763425 | Rare:89 | ||||
chr14:74923195-74923494 | Common:5; Rare:71 | ||||
chr14:75002741-75002947 | Common:1; Rare:59; Clinvar:2 |