Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:63641490-63641578 | Rare:18 | ||||
chr14:63641823-63642172 | Common:5; Rare:115 | ||||
chr14:63728046-63728144 | Common:1; Rare:48 | ||||
chr14:63852869-63853061 | Common:1; Rare:74; Clinvar:2; Clinvar (benign):2 | ||||
chr14:64388244-64388401 | Common:2; Rare:81 | ||||
chr14:64503597-64503887 | Common:2; Rare:111 | ||||
chr14:64504548-64504879 | Rare:100 | ||||
chr14:64505230-64505369 | Rare:34 | ||||
chr14:64914274-64914529 | Common:1; Rare:99 | ||||
chr14:64986746-64986954 | Common:1; Rare:78 | ||||
chr14:64987080-64987305 | Rare:80 | ||||
chr14:65102452-65102858 | Common:7; Rare:108; Clinvar:1 | ||||
chr14:65411747-65411937 | Common:2; Rare:53 | ||||
chr14:65412547-65412880 | Common:5; Rare:109 | ||||
chr14:66507807-66508194 | Rare:155 |