chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1141874744141874745G15GENIChomozygous127439479
1141875874141875875TC14GENIChomozygous108262001
1141877015141877015CG13GENIChomozygous130823656
1141877608141877609AG15GENIChomozygous108262015
1141880006141880007CT17GENIChomozygous108262017
1141882243141882244AT24GENIChomozygous108262041
1141882312141882312G15GENIChomozygous127439485
1141876295141876296CA10GENIChomozygous109327770
1141876467141876468GA18GENIChomozygous109327771
1141877152141877153A12GENICheterozygous134357545
1141882348141882348G11GENIChomozygous127439486
1141882352141882353GT12GENIChomozygous121086506
1141882354141882355A12GENIChomozygous127439487
1141882377141882377T11GENIChomozygous127439488
1141882390141882391TC11GENIChomozygous108262045
1141887521141887522A12GENIChomozygous130823657
1141890423141890424AG20GENIChomozygous108262093
1141884698141884699CT23GENIChomozygous109327773
1141885436141885437TA16GENIChomozygous108262069
1141887085141887086GA14GENICpossibly homozygous109327774