Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:77457950-77458160 | Rare:59 | ||||
chr14:77458500-77458765 | Common:1; Rare:48 | ||||
chr14:77616561-77616728 | Common:2; Rare:57; Clinvar:2; Clinvar (benign):3 | ||||
chr14:77616738-77617177 | Common:1; Rare:104; Clinvar (benign):2 | ||||
chr14:77707932-77708186 | Common:2; Rare:129 | ||||
chr14:77760673-77760815 | Rare:60 | ||||
chr14:77760978-77761336 | Common:2; Rare:128 | ||||
chr14:77800001-77800173 | Rare:35 | ||||
chr14:77800175-77800561 | Common:4; Rare:79 | ||||
chr14:80941639-80942000 | Common:5; Rare:87 | ||||
chr14:81220778-81221530 | Common:4; Rare:264 | ||||
chr14:81533742-81534013 | Common:1; Rare:76 | ||||
chr14:87992851-87992982 | Common:1; Rare:50; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
chr14:87993037-87993427 | Common:5; Rare:172; Clinvar:14; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
chr14:88005110-88005207 | Rare:16 |