Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:68259143-68259215 | Rare:30 | ||||
chr17:68511592-68512084 | Common:4; Rare:132 | ||||
chr17:68512302-68512561 | Common:1; Rare:90; Clinvar:2; Clinvar (benign):3 | ||||
chr17:68540848-68541185 | Common:4; Rare:106 | ||||
chr17:68541712-68541966 | Rare:49 | ||||
chr17:68600472-68600637 | Common:2; Rare:58; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr17:69141808-69142040 | Common:2; Rare:49 | ||||
chr17:69327052-69327334 | Common:2; Rare:93 | ||||
chr17:70169300-70169539 | Common:1; Rare:70 | ||||
chr17:72120793-72121034 | Rare:63 | ||||
chr17:73192811-73193076 | Common:15; Rare:110; Clinvar:2; Clinvar (benign):1 | ||||
chr17:73232226-73232711 | Common:3; Rare:175 | ||||
chr17:73311963-73312349 | Rare:101 | ||||
chr17:74213443-74213578 | Common:1; Rare:35 | ||||
chr17:74466578-74466692 | Rare:35 |