chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1141098417141098418TG22GENIChomozygous109327446
1141098439141098440A21GENIChomozygous130823487
1141099192141099192CACGTACACACACACATA14GENIChomozygous130823488
1141099486141099487TG17GENIChomozygous109327447
1141099701141099702GA19GENIChomozygous109327448
1141101421141101422GA12GENIChomozygous109327449
1141102901141102902CT22GENIChomozygous109327450
1141101245141101246AC16GENIChomozygous108260086
1141102193141102194CA17GENIChomozygous108260088
1141102413141102414AC21GENIChomozygous108260090
1141102131141102132A16GENICpossibly homozygous127438798
1141103600141103601AG18GENIChomozygous109327451
1141103747141103747TGGCCTTGTTGGAGTGGGTG13GENIChomozygous127438799
1141103952141103953G10GENIChomozygous127438800
1141104542141104543AG13GENIChomozygous108260098
1141104725141104725A20GENIChomozygous127438801
1141106043141106044CT26GENIChomozygous109327452
1141106076141106077TA20GENIChomozygous109327453
1141106298141106299CT18GENIChomozygous109327454
1141106302141106302A18GENIChomozygous130823489
1141106397141106398GA10GENIChomozygous109327455
1141106747141106748GA4GENIChomozygous109327457
1141106807141106807CC1GENIChomozygous130823490
1141107668141107669GT19GENIChomozygous109327458
1141107707141107708TC17GENIChomozygous109327459
1141107758141107759AG20GENIChomozygous109327460
1141108119141108120CT26GENIChomozygous108260106
1141108415141108416GA26GENIChomozygous109327461
1141108916141108917GA19GENIChomozygous109327462
1141110129141110130CT13GENIChomozygous109327463
1141110156141110157C11GENIChomozygous130823491
1141110159141110161AC11GENIChomozygous130823492
1141110595141110596CG29GENIChomozygous109327464
1141111118141111119CT10GENIChomozygous109327465
1141106827141106828CT1GENIChomozygous130846347