chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101357652913576530GA23GENIChomozygous142217899
101357830913578310A13GENIChomozygous403276848
101357830913578310AC13GENICheterozygous403276849
101357831013578311A13GENICheterozygous403276850
101357831013578311AC13GENIChomozygous403276851
101357885013578851TC10GENIChomozygous142217900
101357905913579060CT16GENIChomozygous142217901
101357926013579261CA15GENIChomozygous142217902
101357950313579503A25GENIChomozygous142196775
101357882513578833TTTTCTTT10GENIChomozygous142196771
101357883613578836T10GENIChomozygous142196772
101357904913579050G16GENIChomozygous142196773
101357922413579224G13GENIChomozygous142196774
101358026013580260T12GENIChomozygous142196776
101358094513580946TC14GENIChomozygous142217903
101358303313583034TC19GENIChomozygous142217905
101358532813585329AT17GENIChomozygous142217906
101358548513585486CT19GENIChomozygous142217907
101358719713587197TTTTTTTG9GENICheterozygous142196777
101359013813590139TC23GENIChomozygous142217908
101359391213593913AG16GENIChomozygous142217909
101359409213594093AC16GENICpossibly homozygous403276852
101359409213594093A16GENICheterozygous403276853
101359451913594520AG29GENIChomozygous142217911
101359470213594703GA23GENIChomozygous142217912
101359799913598000TC24GENICpossibly homozygous142217913
101360029013600291AG34GENIChomozygous142217914
101360702013607021AG20GENIChomozygous142217915
101360713013607131TC19GENIChomozygous142217916
101360713713607138AC20GENIChomozygous142217917
101361055613610557AG18GENIChomozygous142217918
101361612613616127TC19GENIChomozygous142217919
101361699913617000GC23GENIChomozygous142217920
101361762513617626G10GENIChomozygous145148018
101358156413581565GA16GENIChomozygous145734297
101359410013594101AC15GENICpossibly homozygous138725959
101359411313594113C14GENIChomozygous144853624