chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85970017959700179T60GENICpossibly homozygous141015815
85970129459701295CT53GENIChomozygous141027576
85970140459701405CA54GENIChomozygous141027577
85970152059701521AG60GENICpossibly homozygous141027578
85970179259701793TC52GENIChomozygous141027579
85970308759703088GA30GENIChomozygous141027580
85970442259704423AT39GENIChomozygous141027581
85970478359704784TC62GENIChomozygous141027582
85970649559706496CT57GENIChomozygous141027583
85970778459707785CG53GENIChomozygous141027584
85971116359711164AG44GENICpossibly homozygous141027585
85971197759711978CT51GENIChomozygous141027586
85971242159712422AG50GENICpossibly homozygous141027587
85971444059714441TC37GENIChomozygous141027588
85971672859716728CGCA21GENICheterozygous141015816
85971673059716730CA21GENICpossibly homozygous141015817
85971709559717096AC46GENIChomozygous141027589
85971780159717802GA53GENIChomozygous141027590
85971958159719582AG45GENIChomozygous141027591
85971964159719642TC49GENIChomozygous141027592
85972165059721651TC43GENIChomozygous141027593
85972239359722394CT38GENIChomozygous141027594
85972367459723675TA50GENIChomozygous141027595
85972374259723743CT46GENIChomozygous141027596
85972413259724133TG52GENIChomozygous141027597
85972509659725104TTTGCTTG40GENICpossibly homozygous141015818
85972593059725931GA45GENIChomozygous141027598
85972653959726539T48GENIChomozygous141015819
85972657459726575CT45GENIChomozygous141027599