Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:45253065-45253312 | Rare:69 | ||||
chr14:45253480-45253609 | Common:2; Rare:56 | ||||
chr14:49586289-49586776 | Common:1; Rare:247; Clinvar (benign):1 | ||||
chr14:49598663-49599062 | Common:2; Rare:147 | ||||
chr14:49620563-49620820 | Common:2; Rare:103; Clinvar:1 | ||||
chr14:49893048-49893142 | Rare:34 | ||||
chr14:50312189-50312380 | Rare:77 | ||||
chr14:50396819-50396999 | Common:3; Rare:53 | ||||
chr14:50532474-50532798 | Common:3; Rare:102 | ||||
chr14:50561120-50561196 | Rare:14 | ||||
chr14:50668295-50668563 | Common:4; Rare:100 | ||||
chr14:50944399-50944559 | Common:4; Rare:60; Clinvar:1; Clinvar (benign):2 | ||||
chr14:51239973-51240314 | Common:2; Rare:117 | ||||
chr14:51651454-51651481 | Rare:12 | ||||
chr14:51651627-51652153 | Common:6; Rare:147 |