Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:49586317-49586802 | Common:1; Rare:252; Clinvar (benign):1 | ||||
chr14:49598657-49598722 | Rare:28 | ||||
chr14:49598731-49599061 | Common:1; Rare:118 | ||||
chr14:49620561-49620833 | Common:2; Rare:112; Clinvar:3 | ||||
chr14:49688199-49688266 | Rare:23 | ||||
chr14:49892889-49893211 | Rare:129 | ||||
chr14:50312146-50312376 | Rare:101 | ||||
chr14:50396819-50396976 | Common:2; Rare:44 | ||||
chr14:50532455-50532810 | Common:4; Rare:107 | ||||
chr14:50532931-50533087 | Common:1; Rare:39 | ||||
chr14:50668295-50668556 | Common:3; Rare:95 | ||||
chr14:50944305-50944571 | Common:5; Rare:98; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr14:51240009-51240360 | Common:2; Rare:127 | ||||
chr14:51488865-51489240 | Common:1; Rare:71 | ||||
chr14:51651613-51652175 | Common:6; Rare:152 |