chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18433963184339632TC22GENIChomozygous108880365
18434010584340106CT32GENIChomozygous109503777
18434084684340847TC32GENIChomozygous108880367
18434112884341129CT40GENIChomozygous109503778
18434166084341661CT40GENIChomozygous109503779
18434174684341747TC54GENIChomozygous108880370
18434187984341880CT56GENIChomozygous109503780
18434196384341964CT46GENIChomozygous109503781
18434196784341968AG50GENIChomozygous108880371
18434324184343242AT30GENIChomozygous108880376
18434372884343729TC58GENICpossibly homozygous108880378
18434395784343958GA54GENIChomozygous109503782
18434421284344213AT37GENIChomozygous108880380
18434463184344632TG41GENIChomozygous108880384
18434500084345001GC55GENIChomozygous109503783
18434613084346131AG34GENIChomozygous108880393
18434940184349402CT43GENIChomozygous109503784
18435129484351295AG35GENICpossibly homozygous108880414
18435257684352577CT45GENIChomozygous108880416
18435275884352759AG42GENIChomozygous108880417
18435305984353060CT38GENIChomozygous109503785
18435332084353321AG53GENIChomozygous109503786
18435344484353445CT39GENIChomozygous109503787
18435416884354169CT45GENIChomozygous109503788
18435431384354314TC30GENIChomozygous109503789
18435527284355273AC44GENIChomozygous109503790
18435619284356193TC58GENIChomozygous108880422
18435721384357214TC55GENIChomozygous108880423
18435902984359030AG47GENICpossibly homozygous109503791
18435966184359662AC52GENIChomozygous109503792
18435969684359697TC48GENIChomozygous109503793
18436011684360117AT32GENIChomozygous109503794
18436018084360181GA15GENIChomozygous109503795
18436022784360228GT35GENIChomozygous108880426
18436037484360375GA46GENIChomozygous108880427
18436039584360396CA34GENICpossibly homozygous108880428
18436099784360998GC40GENIChomozygous108880429
18436164084361641CT37GENICpossibly homozygous108880431