chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1456171405617141AC9GENIChomozygous113802266
1456212095621210GT27GENICpossibly homozygous113571118
1456295945629595CA26GENIChomozygous113571119
1456300635630064GC7GENIChomozygous113322573
1456505495650550CT24GENIChomozygous113322574
1457014645701465AC31GENICheterozygous113322575
1457015815701582AG39GENICheterozygous113322581
1457016275701628GA33GENICheterozygous113322582
1457016845701685CA34GENICheterozygous113322584
1457017475701748CA36GENICheterozygous113322585
1457017525701753TA31GENICheterozygous113322586
1457017605701761GC26GENICheterozygous113322587
1457019905701991CT9GENIChomozygous113322589
1457020065702007AT13GENICheterozygous113322590
1457020355702036TG17GENICheterozygous113322591
1457020575702058CG26GENICheterozygous113322592
1457022955702296CA45GENICheterozygous113571123
1457023215702322TA40GENICheterozygous113322593
1457023825702383TG40GENICheterozygous113322594
1457025555702556TC33GENICheterozygous113322595
1457025615702562CG32GENICheterozygous113322596
1457025685702569TC33GENICheterozygous113322597
1457025825702583GA26GENICheterozygous113322598
1457026375702638CT27GENICheterozygous113322601
1457027075702708TC19GENICheterozygous113322602
1457027235702724GC13GENICheterozygous113322603
1457029045702905CT21GENIChomozygous113571124
1457029445702945GA31GENICheterozygous113846088
1457029635702964TC36GENIChomozygous113571125
1457032375703238AG21GENIChomozygous113571126
1457032875703288CT28GENICheterozygous113322604
1457033195703320TC29GENICheterozygous113322605
1457034465703447AG29GENICheterozygous113322606
1457035945703595GA29GENICheterozygous113322608
1456479135647914TA19GENIChomozygous113712545
1457037205703721GA35GENICheterozygous113322611
1457038105703811TC39GENICheterozygous113322612
1457038285703829TG36GENICheterozygous113322613
1457040145704015CA27GENICheterozygous113322614