chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
55655520956555210CA87GENICpossibly homozygous113811620
55655563956555640GC34GENIChomozygous113811622
55655610056556101TG71GENIChomozygous113811624
55655687156556872AC60GENIChomozygous113811626
55655739456557395TC59GENIChomozygous113811628
55655883856558839AT77GENIChomozygous113811630
55655903656559037AG58GENIChomozygous113811632
55655949856559499AT64GENIChomozygous113811634
55655986656559867TC79GENICpossibly homozygous113811636
55656006956560070GA42GENICheterozygous113811638
55656016356560164CT30GENICheterozygous113811640
55656075656560757CT82GENICheterozygous114117360
55656078356560784AG30GENICpossibly homozygous113811642
55656079556560796CT33GENICheterozygous113811644
55656080256560803CT37GENICheterozygous113811646
55656081356560814AG40GENICheterozygous114117362
55656093156560932CT71GENIChomozygous113811648
55656100456561005AG58GENIChomozygous113811650
55656114056561141GT40GENIChomozygous113811652
55656208056562081CT62GENIChomozygous113811654
55656254656562547TC68GENIChomozygous113811656
55656318756563188TC42GENIChomozygous113811658
55656330756563308TA49GENIChomozygous113811660
55656435356564354CA51GENIChomozygous113811662
55656514356565144TG43GENIChomozygous113811664
55656521156565212AG43GENIChomozygous113811666
55656583756565838CT65GENIChomozygous113811668
55656616956566170TC46GENIChomozygous113811670
55656621356566214GA33GENIChomozygous113811672