chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5131337694131337695CG25GENIChomozygous56451612
5131338329131338330TTAC6GENICheterozygous56451614
5131338330131338332AC--6GENICheterozygous56451616
5131339212131339213GA28GENIChomozygous56451618
5131339215131339216CA28GENIChomozygous56451620
5131339286131339287AT24GENIChomozygous56451622
5131339330131339331AG26GENIChomozygous56451624
5131339700131339701AG32GENIChomozygous56451626
5131341244131341245AG19GENIChomozygous55722153
5131341423131341424GA34GENIChomozygous56451628
5131342028131342029T-34GENIChomozygous56451630
5131342591131342592T-16GENIChomozygous56451632
5131342592131342593TA16GENIChomozygous56451634
5131342735131342736TC20GENIChomozygous55722160
5131342997131342998GT26GENIChomozygous56451636
5131343061131343062TC35GENIChomozygous55722162
5131343298131343299CT34GENIChomozygous56451638
5131343926131343927GA25GENIChomozygous56451639
5131344736131344737AAC38GENIChomozygous56451641
5131345513131345514GC18GENIChomozygous56451643
5131345529131345530AG22GENIChomozygous56451645
5131345639131345640CT23GENIChomozygous56451647
5131345749131345750CA27GENIChomozygous56451649