chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101357652913576530GA26GENIChomozygous142217899
101357830913578310A12GENICpossibly homozygous403276848
101357830913578310AC12GENICheterozygous403276849
101357831013578311A12GENICheterozygous403276850
101357831013578311AC12GENICpossibly homozygous403276851
101357885013578851TC14GENIChomozygous142217900
101357905913579060CT9GENIChomozygous142217901
101357926013579261CA12GENIChomozygous142217902
101357950313579503A21GENIChomozygous142196775
101357882513578833TTTTCTTT14GENIChomozygous142196771
101357883613578836T14GENIChomozygous142196772
101357904913579050G8GENIChomozygous142196773
101357922413579224G16GENIChomozygous142196774
101358026013580260T13GENIChomozygous142196776
101358094513580946TC25GENIChomozygous142217903
101358156513581566GA20GENIChomozygous142217904
101358303313583034TC26GENIChomozygous142217905
101358532813585329AT20GENIChomozygous142217906
101358548513585486CT36GENIChomozygous142217907
101358719713587197TTTTTTTG12GENIChomozygous142196777
101359013813590139TC28GENIChomozygous142217908
101359391213593913AG22GENIChomozygous142217909
101359409213594093AC11GENIChomozygous403276852
101359409213594093A11GENICheterozygous403276853
101359451913594520AG28GENIChomozygous142217911
101359470213594703GA25GENIChomozygous142217912
101359799913598000TC26GENIChomozygous142217913
101360029013600291AG19GENIChomozygous142217914
101360702013607021AG29GENIChomozygous142217915
101360713013607131TC28GENIChomozygous142217916
101360713713607138AC28GENIChomozygous142217917
101361055613610557AG23GENIChomozygous142217918
101361612613616127TC19GENIChomozygous142217919
101361699913617000GC31GENIChomozygous142217920
101358854013588541CT29GENIChomozygous144859391
101359410013594101AC13GENIChomozygous138725959
101359411313594113C15GENIChomozygous144853624