chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1171621830171621831T11GENIChomozygous130214765
1171651073171651073AA12GENIChomozygous130214766
1171669011171669013GG21GENIChomozygous127456042
1171669017171669017T19GENIChomozygous127456043
1171669021171669022G20GENIChomozygous127456044
1171669024171669025C21GENIChomozygous127456045
1171669036171669036T19GENIChomozygous127456046
1171669166171669167T18GENIChomozygous127456047
1171676681171676682GA15GENICheterozygous127563866
1171623055171623056AG28GENICheterozygous130736832
1171623059171623060CT28GENICheterozygous130736833
1171623065171623066GA28GENICheterozygous130736834
1171676697171676698GA14GENICheterozygous130736835
1171623069171623070T28GENICheterozygous130731966
1171676760171676761TC20GENICheterozygous130736839
1171676720171676721GA16GENICheterozygous130736836
1171676735171676736AT17GENICheterozygous130736837
1171676748171676749CA19GENICheterozygous130736838
1171676967171676968TG25GENICheterozygous108378621
1171676988171676989CG25GENICheterozygous108755437
1171676990171676991CA25GENICheterozygous108755438
1171677155171677156TC29GENICheterozygous108959659
1171677158171677159CT29GENICheterozygous127563870
1171677285171677286AG19GENICheterozygous108378643
1171693475171693476G9GENICheterozygous130731967
1171726564171726565CT1GENIChomozygous130736840
1171768034171768035T4GENIChomozygous127456080
1171768040171768040G4GENIChomozygous127456081
1171768053171768054G3GENIChomozygous127456082
1171768067171768067C6GENIChomozygous127456083