Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:2068901-2069135 | Common:2; Rare:65 | ||||
chr17:3663785-3664058 | Rare:67 | ||||
chr17:8326548-8326754 | Rare:47 | ||||
chr17:16439533-16439679 | Rare:59 | ||||
chr17:17685863-17686076 | Common:1; Rare:42 | ||||
chr17:17836139-17836418 | Common:3; Rare:71 | ||||
chr17:39729698-39729828 | Common:1; Rare:32 | ||||
chr17:41775543-41775659 | Common:1; Rare:28 | ||||
chr17:43315656-43315916 | Common:6; Rare:110 | ||||
chr17:50189892-50190074 | Common:1; Rare:53; Clinvar:2; Clinvar (benign):4 | ||||
chr17:58631834-58632132 | Common:3; Rare:125 | ||||
chr17:60134871-60135039 | Rare:26 | ||||
chr17:64385336-64385507 | Common:1; Rare:25 | ||||
chr17:64781511-64781711 | Common:2; Rare:54 | ||||
chr17:64837105-64837285 | Common:1; Rare:47 |