chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18433942884339429GA23GENIChomozygous108880363
18433963184339632TC23GENIChomozygous108880365
18433989984339900GT24GENICpossibly homozygous120868687
18434070784340708GA16GENICpossibly homozygous108880366
18434084684340847TC19GENIChomozygous108880367
18434099384340994TA29GENICpossibly homozygous108880368
18434174684341747TC31GENICpossibly homozygous108880370
18434187984341880CT25GENIChomozygous109503780
18434196784341968AG32GENIChomozygous108880371
18434372884343729TC24GENICpossibly homozygous108880378
18434421284344213AT28GENICpossibly homozygous108880380
18434440684344407AG26GENIChomozygous120868688
18434463184344632TG21GENICpossibly homozygous108880384
18434539484345395AG18GENIChomozygous120868689
18434578784345788TC29GENICpossibly homozygous108880390
18434613084346131AG25GENICpossibly homozygous108880393
18435113684351137GC13GENIChomozygous120868690
18435123884351239CT18GENIChomozygous120868691
18435129484351295AG23GENIChomozygous108880414
18435248884352489CT25GENIChomozygous108880415
18435257684352577CT24GENIChomozygous108880416
18435275884352759AG8GENIChomozygous108880417
18435332084353321AG19GENIChomozygous109503786
18435416884354169CT24GENICpossibly homozygous109503788
18435431384354314TC40GENICpossibly homozygous109503789
18435527284355273AC26GENICpossibly homozygous109503790
18435619284356193TC24GENIChomozygous108880422
18435746184357462TA31GENICpossibly homozygous120868692
18435832584358326CT37GENICpossibly homozygous120868693
18435902984359030AG27GENIChomozygous109503791
18435927984359280CT25GENIChomozygous120868694
18435966184359662AC28GENIChomozygous109503792
18435969684359697TC30GENIChomozygous109503793
18436039584360396CA21GENIChomozygous108880428
18436064984360650AG23GENICpossibly homozygous120868695
18436099784360998GC26GENICpossibly homozygous108880429
18436164084361641CT12GENIChomozygous108880431