chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109538660895386609TC33GENIChomozygous68186957
109538671195386712AG41GENIChomozygous68186961
109538675295386753AT32GENIChomozygous68186964
109538709195387092CT58GENIChomozygous68471394
109538714395387144AG73GENICpossibly homozygous68186967
109538734995387350GA73GENIChomozygous68471397
109538783695387837CG51GENIChomozygous68186971
109538809595388096GA54GENIChomozygous68186974
109538922595389226GA45GENICpossibly homozygous68186986
109539134595391346CT56GENICpossibly homozygous68187053
109539143895391439GA35GENICheterozygous68187057
109539174195391742CT51GENIChomozygous68471403
109539184695391847CT56GENIChomozygous68187065
109539263595392636TC29GENIChomozygous68471410
109539417095394171GA35GENIChomozygous68471414
109539450695394507GA45GENIChomozygous68471417
109539493395394934TC13GENIChomozygous68187096
109539519095395191TC22GENIChomozygous68471420
109539535195395352CT38GENIChomozygous68471423
109539737395397374CT48GENIChomozygous68471428
109539808295398083AG66GENIChomozygous68471432
109539809995398100CT72GENIChomozygous68471435
109539826495398265AG45GENIChomozygous68471438
109539856995398570TC36GENIChomozygous68187119
109539864595398646CT37GENIChomozygous68471440
109539933995399340GA32GENIChomozygous68471443
109539146295391463GA50GENICheterozygous68932563