chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
17826168578261688CAG11GENIChomozygous127397047
17826169378261694C12GENIChomozygous127397048
17826169978261700CG12GENIChomozygous108728727
17826170078261701GA12GENIChomozygous108728728
17826170778261707CA11GENIChomozygous127397049
17826173678261736C13GENIChomozygous127397050
17826173978261740TC13GENIChomozygous108728729
17826175078261750T13GENIChomozygous127397051
17826175578261756C12GENIChomozygous127397052
17826177078261771A14GENIChomozygous127397053
17826178178261782A15GENIChomozygous127397054
17826178778261787T15GENIChomozygous127397055
17826179378261794G15GENIChomozygous127397056
17826180078261800A17GENIChomozygous127397057
17826181178261812GC16GENIChomozygous108728730
17826181378261814C16GENIChomozygous127397058
17826181978261820C17GENIChomozygous127397059
17826185778261858C24GENIChomozygous127397060
17826186578261867TG25GENIChomozygous127397061
17826189478261894G24GENIChomozygous127397062
17826191878261918G25GENIChomozygous127397063
17826192978261930G28GENIChomozygous127397064
17826194078261940G30GENIChomozygous127397065
17826194578261945C30GENIChomozygous127397066
17826199078261990A27GENIChomozygous127397067
17826200278262002T22GENIChomozygous127397068
17826201078262011G17GENIChomozygous127397069
17826201878262019C17GENIChomozygous127397070
17826203278262033A14GENIChomozygous127397071
17826204378262044A14GENIChomozygous127397072
17826205078262051CG12GENIChomozygous120514050
17826205078262050A13GENIChomozygous127397073
17826206278262063TG11GENIChomozygous108139729
17826206878262069T11GENIChomozygous127397074
17826207278262074GA10GENIChomozygous127397075
17826407778264078G2GENIChomozygous127397076
17826408178264086GCGCG2GENIChomozygous127397077
17826409878264098GGC3GENIChomozygous127397078
17826410578264110TGGAG4GENIChomozygous127397079
17826473378264733G20GENIChomozygous131257696