chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101357652913576530GA53GENIChomozygous142217899
101357830913578310A28GENICpossibly homozygous403276848
101357830913578310AC28GENICheterozygous403276849
101357885013578851TC46GENIChomozygous142217900
101357905913579060CT45GENIChomozygous142217901
101357922413579224G52GENIChomozygous142196774
101357831013578311A28GENICheterozygous403276850
101357831013578311AC28GENICheterozygous403276851
101357882513578833TTTTCTTT42GENIChomozygous142196771
101357883613578836T46GENIChomozygous142196772
101357904913579050G40GENIChomozygous142196773
101357926013579261CA46GENIChomozygous142217902
101357950313579503A65GENIChomozygous142196775
101358026013580260T57GENIChomozygous142196776
101358094513580946TC80GENIChomozygous142217903
101358156513581566GA82GENIChomozygous142217904
101358303313583034TC63GENIChomozygous142217905
101358532813585329AT66GENIChomozygous142217906
101358548513585486CT50GENIChomozygous142217907
101358719713587197TTTTTTTG49GENICheterozygous142196777
101358877713588778TG10GENICheterozygous145148743
101359013813590139TC52GENIChomozygous142217908
101359391213593913AG67GENIChomozygous142217909
101359409213594093AC37GENICpossibly homozygous403276852
101359409213594093A37GENICheterozygous403276853
101359410013594101AC38GENICpossibly homozygous138725959
101359451913594520AG57GENIChomozygous142217911
101359470213594703GA54GENIChomozygous142217912
101359799913598000TC65GENIChomozygous142217913
101360029013600291AG79GENIChomozygous142217914
101360702013607021AG67GENIChomozygous142217915
101360713013607131TC84GENIChomozygous142217916
101360713713607138AC84GENIChomozygous142217917
101361055613610557AG71GENIChomozygous142217918
101361612613616127TC65GENIChomozygous142217919
101361699913617000GC93GENIChomozygous142217920
101359411313594113C39GENICpossibly homozygous144853624