chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
12047657920476580AG48GENIChomozygous141199839
12047718920477190AG56GENIChomozygous141199840
12047734720477348AC61GENIChomozygous144532919
12047734820477349GT61GENIChomozygous144532920
12047925620479257AT3GENIChomozygous144532921
12047925820479259AT3GENIChomozygous144532922
12047926020479261AT2GENIChomozygous144532923
12047927520479276GC2GENIChomozygous144532924
12048058520480586AT53GENIChomozygous144532925
12048065620480657GA53GENIChomozygous144532926
12048080820480809GA37GENIChomozygous141199842
12048117320481174GT32GENIChomozygous144532927
12048152320481524AG48GENIChomozygous144532928
12048177520481776AG36GENIChomozygous141199843
12048192920481930TG32GENIChomozygous141199844
12048196020481961GC22GENIChomozygous141199845
12048200920482010AG18GENIChomozygous141199846
12048246820482469TC40GENIChomozygous141199847
12048248720482488CG40GENIChomozygous141199848
12048249120482492GA39GENIChomozygous141199849
12048272620482727TC57GENIChomozygous141199850
12048340220483403GA34GENIChomozygous144532929
12048346820483469GA33GENIChomozygous144532930
12048348120483482GT32GENIChomozygous144532931
12048355620483557AG34GENIChomozygous144532932
12048406220484066AGGA78GENICpossibly homozygous144520113
12048407620484079CAT78GENICpossibly homozygous144520115
12048364120483645AAAA50GENIChomozygous141159360
12048377520483776T37GENIChomozygous141159361
12048331620483317G16GENICpossibly homozygous402941763
12048331620483317GC16GENICheterozygous402941764
12048406820484072GATA78GENICpossibly homozygous144520114
12048419120484192TC51GENIChomozygous144532933
12048420620484207TC47GENIChomozygous141199854
12048695120486951TAATGTT45GENIChomozygous144520116
12048706720487068GA57GENIChomozygous144532934