chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1233777060233777061TG26GENIChomozygous108564189
1233777061233777062CA27GENIChomozygous108564191
1233804830233804831GA22GENIChomozygous108772910
1233809321233809322TG43GENICheterozygous109539226
1233813200233813201TG58GENICheterozygous109539227
1233818307233818308CG42GENIChomozygous108564426
1233820816233820817GT62GENICpossibly homozygous108564436
1233820868233820869AG60GENIChomozygous108564438
1233821857233821858GT14GENIChomozygous108564446
1233821927233821928AT10GENICpossibly homozygous108564448
1233822586233822587GT39GENIChomozygous108564450
1233822656233822657AT33GENIChomozygous108564452
1233832236233832237CG16GENIChomozygous108564484
1233833259233833260CT35GENIChomozygous108564486
1233833458233833459TC42GENIChomozygous108564488
1233833469233833470GT40GENIChomozygous108564490
1233833512233833513CG23GENIChomozygous108564492
1233833582233833583CT37GENIChomozygous108564494
1233833706233833707CT45GENIChomozygous108564496
1233834040233834041AC43GENICpossibly homozygous108564500
1233834549233834550GT40GENIChomozygous108564504
1233834697233834698AG53GENIChomozygous108564506
1233834931233834932GT65GENIChomozygous108564508