chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101357652913576530GA39GENIChomozygous142217899
101357830913578310A21GENICheterozygous403276848
101357830913578310AC21GENICheterozygous403276849
101357831013578311A21GENICheterozygous403276850
101357831013578311AC21GENICheterozygous403276851
101357885013578851TC20GENIChomozygous142217900
101357905913579060CT32GENIChomozygous142217901
101357926013579261CA35GENIChomozygous142217902
101357950313579503A45GENIChomozygous142196775
101357882513578833TTTTCTTT19GENIChomozygous142196771
101357883613578836T20GENIChomozygous142196772
101357904913579050G28GENIChomozygous142196773
101357922413579224G37GENIChomozygous142196774
101358026013580260T36GENIChomozygous142196776
101358094513580946TC41GENIChomozygous142217903
101358303313583034TC52GENIChomozygous142217905
101358532813585329AT39GENIChomozygous142217906
101358548513585486CT33GENIChomozygous142217907
101358719713587197TTTTTTTG37GENICpossibly homozygous142196777
101358877713588778TG5GENIChomozygous145148743
101359013813590139TC46GENIChomozygous142217908
101359409213594093AC32GENIChomozygous403276852
101359409213594093A32GENICheterozygous403276853
101361055613610557AG44GENIChomozygous142217918
101359391213593913AG38GENIChomozygous142217909
101359451913594520AG42GENIChomozygous142217911
101359470213594703GA54GENIChomozygous142217912
101359799913598000TC49GENIChomozygous142217913
101360029013600291AG42GENIChomozygous142217914
101360702013607021AG74GENIChomozygous142217915
101360713013607131TC62GENIChomozygous142217916
101360713713607138AC61GENIChomozygous142217917
101358156413581565GA27GENIChomozygous145734297
101359408013594086AAAAAC24GENICheterozygous145727668
101359410013594101AC38GENIChomozygous138725959
101359411313594113C38GENICpossibly homozygous144853624
101361612613616127TC61GENIChomozygous142217919
101361699913617000GC41GENIChomozygous142217920
101361762513617626G20GENICheterozygous145148018