chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101357652913576530GA16GENIChomozygous142217899
101357830913578310A9GENIChomozygous403276848
101357830913578310AC9GENICheterozygous403276849
101357831013578311A10GENICheterozygous403276850
101357831013578311AC10GENIChomozygous403276851
101357882513578833TTTTCTTT8GENIChomozygous142196771
101357883613578836T8GENIChomozygous142196772
101357885013578851TC8GENIChomozygous142217900
101357904913579050G6GENIChomozygous142196773
101357905913579060CT7GENIChomozygous142217901
101357922413579224G12GENIChomozygous142196774
101357926013579261CA11GENIChomozygous142217902
101357950313579503A17GENIChomozygous142196775
101358026013580260T14GENIChomozygous142196776
101358094513580946TC14GENIChomozygous142217903
101358156513581566GA15GENIChomozygous142217904
101358303313583034TC22GENIChomozygous142217905
101358532813585329AT23GENIChomozygous142217906
101358548513585486CT21GENIChomozygous142217907
101358719713587197TTTTTTTG14GENICpossibly homozygous142196777
101359013813590139TC19GENIChomozygous142217908
101359391213593913AG13GENIChomozygous142217909
101359409313594094AC3GENIChomozygous142217910
101359451913594520AG13GENIChomozygous142217911
101359470213594703GA10GENIChomozygous142217912
101359799913598000TC28GENIChomozygous142217913
101360029013600291AG16GENIChomozygous142217914
101360702013607021AG17GENIChomozygous142217915
101360713013607131TC17GENIChomozygous142217916
101360713713607138AC15GENIChomozygous142217917
101361055613610557AG16GENIChomozygous142217918
101361612613616127TC12GENIChomozygous142217919
101361699913617000GC16GENIChomozygous142217920