Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:64704135-64704275 | Rare:33 | ||||
chr14:64914359-64914680 | Rare:129 | ||||
chr14:64914697-64914894 | Common:2; Rare:54 | ||||
chr14:64972289-64972563 | Common:4; Rare:84 | ||||
chr14:64986706-64986962 | Common:1; Rare:92 | ||||
chr14:64987001-64987340 | Rare:121 | ||||
chr14:65101688-65101796 | Rare:16 | ||||
chr14:65102444-65102924 | Common:9; Rare:127; Clinvar:1; Clinvar (benign):1 | ||||
chr14:65103018-65103186 | Common:1; Rare:31 | ||||
chr14:65411693-65412010 | Common:2; Rare:96 | ||||
chr14:65412258-65412830 | Common:3; Rare:179 | ||||
chr14:65412846-65413142 | Common:3; Rare:73 | ||||
chr14:65413226-65413369 | Rare:37 | ||||
chr14:65413469-65413636 | Common:1; Rare:45 | ||||
chr14:66507491-66507631 | Rare:36 |