chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7144901384144901385CT10GENIChomozygous115946015
7144901562144901563TA18GENIChomozygous115946017
7144901739144901740GA13GENIChomozygous115946018
7144901750144901751AG18GENIChomozygous115946020
7144902015144902016TC8GENIChomozygous115946022
7144902395144902396AG12GENIChomozygous118516009
7144902896144902897GA16GENIChomozygous115946024
7144903174144903175TC20GENIChomozygous115946025
7144903725144903726GA9GENIChomozygous115946029
7144903878144903879GT15GENICheterozygous115946030
7144904067144904068CA12GENIChomozygous115946032
7144904477144904478CT7GENIChomozygous115946034
7144905408144905409GA7GENIChomozygous115946037
7144905824144905825TG28GENIChomozygous118516011
7144907491144907492AG22GENIChomozygous116378354
7144913521144913522CT15GENIChomozygous116378360
7144913789144913790AC4GENIChomozygous115946080
7144915710144915711GC3GENICheterozygous126649059
7144916617144916618AG17GENIChomozygous115946101
7144917115144917116GA10GENIChomozygous115946103
7144917242144917243TC5GENIChomozygous115946105
7144917497144917498CT19GENIChomozygous115946107
7144918908144918909TC8GENIChomozygous115946113
7144919091144919092AG8GENIChomozygous116378364
7144919301144919302GA5GENIChomozygous126649060
7144919480144919481TG16GENIChomozygous116378366
7144919611144919612GA22GENIChomozygous116378368
7144920007144920008CA17GENIChomozygous116378369
7144920174144920175CT6GENIChomozygous116378371
7144920468144920469TC8GENIChomozygous116378373
7144921400144921401GA23GENIChomozygous116378374
7144922182144922183TC14GENIChomozygous115946119
7144922417144922418TC19GENIChomozygous116378376
7144922476144922477AG6GENIChomozygous115946123
7144922737144922738GT33GENIChomozygous116378378
7144923269144923270GA10GENIChomozygous116378380
7144923455144923456GA21GENIChomozygous116378382
7144923642144923643AG23GENIChomozygous115946129
7144925893144925894GA18GENIChomozygous116378384