chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1141098417141098418TG16GENIChomozygous109327446
1141098439141098440A15GENIChomozygous130823487
1141099192141099192CACGTACACACACACATA14GENIChomozygous130823488
1141099486141099487TG18GENIChomozygous109327447
1141099701141099702GA16GENIChomozygous109327448
1141101245141101246AC13GENIChomozygous108260086
1141101421141101422GA13GENIChomozygous109327449
1141102193141102194CA17GENIChomozygous108260088
1141102413141102414AC17GENIChomozygous108260090
1141102901141102902CT14GENIChomozygous109327450
1141103600141103601AG27GENIChomozygous109327451
1141102131141102132A11GENIChomozygous127438798
1141103747141103747TGGCCTTGTTGGAGTGGGTG5GENIChomozygous127438799
1141103952141103953G7GENIChomozygous127438800
1141104542141104543AG20GENIChomozygous108260098
1141104725141104725A16GENIChomozygous127438801
1141106043141106044CT21GENIChomozygous109327452
1141106076141106077TA17GENIChomozygous109327453
1141106298141106299CT23GENIChomozygous109327454
1141106302141106302A21GENICpossibly homozygous130823489
1141106397141106398GA18GENIChomozygous109327455
1141106747141106748GA10GENIChomozygous109327457
1141106807141106807CC3GENIChomozygous130823490
1141107668141107669GT21GENIChomozygous109327458
1141107707141107708TC23GENIChomozygous109327459
1141107758141107759AG22GENIChomozygous109327460
1141108119141108120CT11GENIChomozygous108260106
1141108415141108416GA23GENIChomozygous109327461
1141108916141108917GA34GENIChomozygous109327462
1141110129141110130CT17GENIChomozygous109327463
1141110156141110157C23GENIChomozygous130823491
1141110159141110161AC20GENIChomozygous130823492
1141110595141110596CG20GENIChomozygous109327464
1141111118141111119CT16GENIChomozygous109327465
1141106826141106826TT6GENICheterozygous135095369
1141106827141106828CT7GENICheterozygous130846347