chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101064548010645481GA10GENIChomozygous116493473
101064600610646007AT8GENIChomozygous116493479
101064641410646415CT6GENIChomozygous116493481
101064714810647149GA9GENIChomozygous116493485
101064760910647610AG9GENIChomozygous116493487
101064848510648486AG7GENIChomozygous116493491
101065304910653050TC17GENIChomozygous116493497
101065365110653652CT7GENIChomozygous116734030
101064802110648022CT10GENIChomozygous116734027
101064848410648485CT7GENIChomozygous116734028
101065231610652317GA10GENIChomozygous116734029
101065437110654372AG9GENIChomozygous116734031
101065438610654387CA10GENIChomozygous116734032
101065441310654414CT7GENIChomozygous116734033
101065448510654486CG11GENIChomozygous116493507
101065449410654495AG11GENIChomozygous116493509
101065467110654672GA6GENIChomozygous116493513
101065475410654755AG8GENIChomozygous116734034
101065476810654769TG7GENIChomozygous116734035
101065501110655012AT5GENIChomozygous116493515
101065710310657104TC12GENIChomozygous116493526
101065756010657561AG9GENIChomozygous116734036
101065772410657725CG6GENIChomozygous116493528
101065775710657758CA9GENIChomozygous116493530
101065801910658020TC10GENIChomozygous116493532
101065917210659173GA11GENIChomozygous116493536
101066034810660349AT8GENIChomozygous116493538
101066155310661554CT5GENIChomozygous116493540
101066323910663240TC9GENIChomozygous116493542
101066389510663896CT8GENIChomozygous116493544
101066584110665842GA6GENIChomozygous116493548
101066585210665853CT6GENIChomozygous116493550
101066674410666745AG6GENIChomozygous116493552
101067382010673821CT11GENIChomozygous116493590
101068399210683993GA9GENIChomozygous116493603
101068499710684998TG11GENIChomozygous116493605
101068595410685955GA7GENIChomozygous116734037
101068612210686123TC12GENIChomozygous116734038
101068626810686269GT7GENIChomozygous116493607
101068910110689102AG8GENIChomozygous116734039