chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3105056451105056452GA41GENIChomozygous141523814
3105058084105058085TC60GENIChomozygous136781569
3105058709105058710TC42GENIChomozygous136781572
3105059215105059216AC59GENICpossibly homozygous136781573
3105061188105061189GT54GENIChomozygous136781574
3105061365105061366TC42GENIChomozygous141523815
3105061390105061391GC46GENIChomozygous136781575
3105061391105061392CT46GENIChomozygous136781576
3105061476105061477CA61GENIChomozygous136781577
3105062496105062497AG45GENIChomozygous136781578
3105063132105063133AT45GENIChomozygous136781579
3105063499105063500GC47GENIChomozygous136781580
3105063548105063549AG57GENIChomozygous136781581
3105063575105063576GC67GENIChomozygous136781582
3105063590105063591AT71GENIChomozygous136781583
3105064114105064115GT61GENIChomozygous136781584
3105065006105065007TC56GENIChomozygous136781585
3105065328105065329AG53GENIChomozygous136781586
3105065696105065697AT57GENIChomozygous136781587
3105067227105067228AG61GENIChomozygous136781589
3105067592105067593CA49GENIChomozygous136781590
3105067994105067995CT49GENIChomozygous141523816
3105067998105067999GA50GENIChomozygous136781591
3105068497105068498GA32GENIChomozygous136781592
3105070637105070638CA70GENIChomozygous141523817
3105068561105068561T13GENICheterozygous136581543
3105061009105061013CACA39GENIChomozygous136581540
3105063114105063126CAGAAAGCAAAC42GENIChomozygous136581541
3105067220105067220TTGAC54GENIChomozygous136581542
3105068560105068560CTT13GENICheterozygous144630489