Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:73886781-73886877 | Common:1; Rare:30 | ||||
chr14:74019277-74019411 | Common:1; Rare:51 | ||||
chr14:74493570-74493770 | Common:3; Rare:76; Clinvar (benign):4 | ||||
chr14:74713085-74713203 | Rare:58 | ||||
chr14:75126998-75127131 | Rare:47 | ||||
chr14:75661175-75661282 | Common:2; Rare:29 | ||||
chr14:76762627-76762836 | Rare:61 | ||||
chr14:77320854-77321048 | Rare:58; Clinvar:1 | ||||
chr14:77457526-77457869 | Common:1; Rare:109 | ||||
chr14:77707981-77708110 | Rare:66 | ||||
chr14:85529937-85530267 | Common:2; Rare:66 | ||||
chr14:89954665-89954960 | Rare:87 | ||||
chr14:90397838-90398010 | Rare:43 | ||||
chr14:90403833-90403899 | Rare:13 | ||||
chr14:92121666-92121985 | Common:4; Rare:105 |