chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1019780710197808TC32GENIChomozygous108224079
X1019856710198568AG26GENIChomozygous108224081
X1019907110199072CA23GENIChomozygous108540398
X1020017810200179T27GENIChomozygous129719527
X1020031210200313GT11GENIChomozygous108730053
X1020138010201381AG32GENIChomozygous108540400
X1020291910202920CT26GENIChomozygous108224083
X1020345210203453TC27GENIChomozygous108224085
X1020441310204414CT21GENIChomozygous108540402
X1020465010204651GA25GENIChomozygous108224089
X1020549910205500GA24GENIChomozygous108540404
X1020699610206997GA28GENIChomozygous108540406
X1020820910208210GT24GENIChomozygous133358340
X1020866310208664CT17GENIChomozygous108540408
X1020907510209076AG21GENIChomozygous108224093
X1020926710209268GA15GENIChomozygous108224095
X1021063810210639TA29GENICpossibly homozygous108730055
X1021082810210829GA25GENIChomozygous108224103
X1021090410210910GACTGC21GENIChomozygous133352855
X1021282210212823CA25GENIChomozygous108730058
X1021311610213117TC29GENIChomozygous108224114
X1021311810213119CT29GENIChomozygous108540410
X1021411710214118CT26GENIChomozygous108540412
X1021488810214889CG5GENIChomozygous133358341
X1021560910215610CT17GENIChomozygous108224116
X1021717610217177AG28GENIChomozygous108366665
X1021777110217772AG27GENIChomozygous108224118