chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1141098417141098418TG13GENIChomozygous109327446
1141098439141098440A12GENIChomozygous130823487
1141099192141099192CACGTACACACACACATA12GENIChomozygous130823488
1141099486141099487TG22GENIChomozygous109327447
1141099701141099702GA24GENIChomozygous109327448
1141101245141101246AC23GENIChomozygous108260086
1141101421141101422GA21GENIChomozygous109327449
1141102193141102194CA11GENIChomozygous108260088
1141102413141102414AC17GENIChomozygous108260090
1141102901141102902CT7GENIChomozygous109327450
1141103600141103601AG17GENIChomozygous109327451
1141102131141102132A9GENICpossibly homozygous127438798
1141103747141103747TGGCCTTGTTGGAGTGGGTG9GENIChomozygous127438799
1141104542141104543AG12GENIChomozygous108260098
1141104725141104725A23GENIChomozygous127438801
1141106043141106044CT22GENIChomozygous109327452
1141106076141106077TA19GENIChomozygous109327453
1141106298141106299CT19GENIChomozygous109327454
1141106302141106302A17GENIChomozygous130823489
1141106397141106398GA11GENIChomozygous109327455
1141106747141106748GA4GENIChomozygous109327457
1141106807141106807CC5GENIChomozygous130823490
1141107668141107669GT23GENIChomozygous109327458
1141107707141107708TC20GENIChomozygous109327459
1141107758141107759AG23GENIChomozygous109327460
1141108119141108120CT24GENIChomozygous108260106
1141108415141108416GA26GENIChomozygous109327461
1141108916141108917GA19GENIChomozygous109327462
1141110129141110130CT11GENIChomozygous109327463
1141110156141110157C17GENIChomozygous130823491
1141110159141110161AC17GENIChomozygous130823492
1141110595141110596CG21GENIChomozygous109327464
1141111118141111119CT17GENIChomozygous109327465
1141107530141107530TTATTTTTT5GENICheterozygous134357540
1141106827141106828CT6GENIChomozygous130846347