chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
139046794190467942CT7GENIChomozygous114574507
139046806790468068AG11GENIChomozygous114693393
139046831790468318AG12GENIChomozygous114574509
139046890890468909GA13GENIChomozygous114574511
139047130790471308TC28GENIChomozygous114574513
139047867690478677AC26GENIChomozygous114574515
139048761190487612TC16GENIChomozygous114693395
139049339290493393CT12GENIChomozygous114574517
139049655590496556GA23GENIChomozygous114574519
139050269890502699GA20GENIChomozygous114574521
139050384490503845GA26GENIChomozygous114574525
139050437790504378CG20GENIChomozygous114574527
139050520490505205CT20GENIChomozygous114574529
139050708290507083CT19GENIChomozygous114574531
139050710390507104GA17GENIChomozygous114574533
139050713090507131CT20GENIChomozygous114574535
139049868690498687CT23GENICpossibly homozygous118536796
139048101090481011GA18GENIChomozygous114424390
139050674190506742CA11GENIChomozygous118465739