Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:50143175-50143325 | Common:1; Rare:23 | ||||
chr14:50201026-50201339 | Common:1; Rare:68 | ||||
chr14:50229253-50229499 | Common:2; Rare:44 | ||||
chr14:50429461-50429687 | Rare:29 | ||||
chr14:50453183-50453269 | Rare:11 | ||||
chr14:50453300-50453347 | Rare:6 | ||||
chr14:50456464-50456477 | Rare:2 | ||||
chr14:50459816-50459889 | Rare:14 | ||||
chr14:50466581-50466693 | Rare:25 | ||||
chr14:50466853-50467062 | Rare:36 | ||||
chr14:50468484-50468784 | Common:1; Rare:60 | ||||
chr14:50479046-50479384 | Common:3; Rare:61 | ||||
chr14:50479447-50479598 | Rare:26 | ||||
chr14:50542061-50542314 | Common:1; Rare:44 | ||||
chr14:50792607-50792757 | Common:1; Rare:49; Clinvar:1 |