chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117538896117538897CT13GENIChomozygous116341568
7117539236117539237TC35GENIChomozygous115847461
7117539592117539593CA35GENIChomozygous115847463
7117540203117540204TC26GENIChomozygous115847467
7117540373117540374CT9GENIChomozygous116341570
7117541710117541711CT24GENIChomozygous115847475
7117544059117544060GA28GENIChomozygous116341572
7117545791117545792TC17GENIChomozygous115847477
7117546373117546374GA4GENIChomozygous116341574
7117546547117546548GC10GENIChomozygous115847479
7117547654117547655CT19GENIChomozygous116341576
7117547846117547847CG22GENIChomozygous115847487
7117550832117550833GA27GENIChomozygous116341580
7117550891117550892AG20GENIChomozygous115847499
7117553239117553240TA16GENICheterozygous115847521
7117553946117553947AG21GENIChomozygous115847523
7117557906117557907GT27GENIChomozygous115847535