Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:75522378-75522628 | Rare:50 | ||||
chr14:75578307-75578701 | Common:2; Rare:79; Clinvar (benign):1 | ||||
chr14:75660819-75660962 | Rare:36 | ||||
chr14:75661167-75661320 | Common:2; Rare:42 | ||||
chr14:76151818-76151984 | Rare:59 | ||||
chr14:76762544-76762935 | Rare:113 | ||||
chr14:77320818-77321094 | Rare:88; Clinvar:3 | ||||
chr14:77376976-77377398 | Common:5; Rare:117 | ||||
chr14:77457542-77457886 | Common:2; Rare:101 | ||||
chr14:77616461-77617083 | Common:3; Rare:170; Clinvar:6; Clinvar (benign):5 | ||||
chr14:77707977-77708188 | Common:2; Rare:111 | ||||
chr14:77737042-77737331 | Common:2; Rare:56 | ||||
chr14:77761091-77761193 | Rare:48 | ||||
chr14:81220708-81221069 | Common:3; Rare:141 | ||||
chr14:81221220-81221347 | Rare:20 |