chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47751936177519362GA79GENIChomozygous112736138
47752114177521142CT54GENIChomozygous113351173
47752323877523239AG58GENIChomozygous112736142
47752527377525274CT60GENIChomozygous112736148
47752625177526252CT50GENIChomozygous113351174
47752817777528178AG54GENIChomozygous112736150
47752832177528322GC43GENIChomozygous119498987
47752832877528329CT43GENIChomozygous119498989
47752918277529183CA51GENIChomozygous112736154
47752957477529575GA49GENIChomozygous112736156
47753184077531841GA59GENIChomozygous112736158
47753198177531982GA62GENIChomozygous112736160
47753233977532340TA61GENIChomozygous112736162
47753240777532408GT49GENIChomozygous112736164
47753461977534620AT75GENIChomozygous112736166
47753513077535131TA42GENIChomozygous112736168
47753715477537155TC51GENIChomozygous112736172
47753731577537316AG58GENIChomozygous112736174
47753964877539649AG59GENIChomozygous112736176
47754162777541628TC64GENIChomozygous112736178
47754579877545798A55GENIChomozygous128051970
47753424077534241T41GENIChomozygous128051964
47752465777524657T49GENIChomozygous128051960
47752579977525801GG40GENIChomozygous128051961
47753392677533926AG25GENIChomozygous128051963
47753674677536750TTAC64GENIChomozygous128051965
47754035477540356CA28GENICpossibly homozygous128051967
47754174677541746GTTTCA53GENIChomozygous128051968
47754537577545377GG57GENIChomozygous128051969
47752834077528341CT39GENIChomozygous113239562
47753095377530957TTCC42GENIChomozygous133729715
47753424277534243CA42GENIChomozygous119278332
47754537777545378GA57GENIChomozygous119278334
47753927877539279AG49GENIChomozygous113276693
47753927977539280TA48GENIChomozygous113276694