chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1192169739192169740G62GENIChomozygous130829624
1192169962192169962A52GENIChomozygous130829625
1192170966192170967GT50GENIChomozygous109180212
1192171888192171889GC53GENIChomozygous120511395
1192172654192172655TA57GENICpossibly homozygous120511396
1192172714192172715CT54GENICpossibly homozygous120511397
1192173045192173046CT49GENIChomozygous108468113
1192173053192173054TC51GENIChomozygous108468114
1192173062192173063TA49GENIChomozygous109180214
1192173035192173036A46GENIChomozygous127467946
1192173069192173070G51GENIChomozygous127467947
1192173063192173064AG50GENIChomozygous120488556
1192173092192173093T50GENIChomozygous127467948
1192173096192173097CA52GENIChomozygous108468115
1192173102192173103AC52GENIChomozygous120488557
1192173103192173104CA51GENIChomozygous120488558
1192173110192173111T52GENIChomozygous127467949
1192173147192173147G50GENIChomozygous127467950
1192173153192173153G50GENIChomozygous127467951
1192173196192173196A42GENIChomozygous127467952
1192173203192173204CA39GENIChomozygous108468116
1192173218192173220GA40GENIChomozygous127467953
1192173224192173224G37GENIChomozygous127467954