Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:68600490-68600641 | Common:2; Rare:52; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr17:68955309-68955471 | Rare:33 | ||||
chr17:69141787-69141936 | Rare:37 | ||||
chr17:69268745-69268930 | Rare:34 | ||||
chr17:70169238-70169539 | Common:1; Rare:77 | ||||
chr17:72120793-72121029 | Rare:62 | ||||
chr17:73232210-73232707 | Common:3; Rare:183 | ||||
chr17:74431264-74431407 | Rare:35 | ||||
chr17:74431984-74432141 | Common:1; Rare:73 | ||||
chr17:74443010-74443086 | Common:2; Rare:17 | ||||
chr17:74466432-74466692 | Rare:65 | ||||
chr17:74776250-74776550 | Common:4; Rare:98 | ||||
chr17:75012605-75012740 | Common:1; Rare:44 | ||||
chr17:75046923-75047320 | Common:2; Rare:126 | ||||
chr17:75109878-75109981 | Common:1; Rare:25 |