chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5147855064147855065CT46GENIChomozygous122415416
5147855142147855142A46GENIChomozygous128253993
5147855160147855161G48GENIChomozygous128253994
5147855193147855193A48GENIChomozygous128253995
5147855197147855198T47GENIChomozygous128253996
5147855252147855253TG52GENIChomozygous114153182
5147855253147855254GT52GENIChomozygous118846561
5147855336147855337TG44GENIChomozygous114153183
5147855337147855338GA44GENIChomozygous114153184
5147856694147856696TT26GENICpossibly homozygous128253997
5147856774147856775C17GENICheterozygous128253998
5147867017147867018TA10GENIChomozygous114348522
5147867020147867023ATG10GENIChomozygous128254002
5147867030147867031TC9GENIChomozygous118846563
5147867031147867032TA7GENIChomozygous118913345
5147867033147867034TC7GENIChomozygous118913347
5147867035147867036TC6GENIChomozygous118913349
5147867038147867041CTA5GENIChomozygous128254003
5147867044147867044A4GENIChomozygous128254004
5147867046147867047CA4GENIChomozygous122415438
5147867057147867058T2GENIChomozygous128254005
5147867155147867156G7GENIChomozygous129917426
5147867164147867165G9GENIChomozygous129917427
5147867170147867171G10GENIChomozygous129917428
5147867176147867176AA11GENIChomozygous129917429
5147867179147867181TG13GENIChomozygous129917430
5147867197147867199GG19GENIChomozygous129917431
5147867206147867208GG21GENIChomozygous129917432
5147867251147867255TATG36GENIChomozygous130315464
5147867127147867129TT4GENIChomozygous130315460
5147867134147867136TG4GENIChomozygous130315461
5147867233147867234C35GENIChomozygous130315462
5147867247147867248T36GENIChomozygous130315463
5147867129147867130TC4GENIChomozygous130323611
5147867264147867265G36GENIChomozygous130315465
5147867275147867275C36GENIChomozygous130315466
5147867577147867577T13GENIChomozygous128254006
5147867584147867585G15GENIChomozygous128254007
5147867590147867591A17GENIChomozygous128254008
5147867600147867602TA18GENIChomozygous128254009