chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47751936177519362GA18GENIChomozygous112736138
47752114177521142CT14GENIChomozygous113351173
47752323877523239AG24GENIChomozygous112736142
47752527377525274CT14GENIChomozygous112736148
47752625177526252CT14GENIChomozygous113351174
47752817777528178AG20GENIChomozygous112736150
47752918277529183CA24GENIChomozygous112736154
47752957477529575GA21GENIChomozygous112736156
47752465777524657T26GENIChomozygous128051960
47752579977525801GG16GENIChomozygous128051961
47752832177528322GC19GENICpossibly homozygous119498987
47752832877528329CT19GENICpossibly homozygous119498989
47752834077528341CT17GENICpossibly homozygous113239562
47753184077531841GA21GENIChomozygous112736158
47753198177531982GA20GENIChomozygous112736160
47753211877532240AGAAATTGTGGCACTGGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCACAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAGACCCAAAAAAAAAAAAAAAAAAA7GENIChomozygous128051962
47753233977532340TA21GENIChomozygous112736162
47753240777532408GT22GENIChomozygous112736164
47753392677533926AG8GENIChomozygous128051963
47753424077534241T19GENIChomozygous128051964
47753461977534620AT21GENIChomozygous112736166
47753513077535131TA17GENIChomozygous112736168
47753674677536750TTAC18GENIChomozygous128051965
47753715477537155TC16GENIChomozygous112736172
47753731577537316AG22GENIChomozygous112736174
47753964877539649AG22GENIChomozygous112736176
47754035477540356CA12GENIChomozygous128051967
47754162777541628TC24GENIChomozygous112736178
47754174677541746GTTTCA19GENIChomozygous128051968
47754537577545377GG24GENIChomozygous128051969
47754579877545798A21GENIChomozygous128051970
47753424277534243CA19GENIChomozygous119278332
47754537777545378GA24GENIChomozygous119278334
47753927877539279AG18GENIChomozygous113276693
47753927977539280TA19GENIChomozygous113276694