chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1200037846200037847CG12GENIChomozygous992707528
1200090493200090494TC42GENICpossibly homozygous992707529
1200091092200091093CT20GENICpossibly homozygous992707530
1200091616200091617CA23GENIChomozygous992707531
1200092336200092337TC36GENIChomozygous992707532
1200093001200093002GT33GENIChomozygous992707533
1200096126200096127AG24GENICpossibly homozygous992707534
1200101883200101884TA22GENICpossibly homozygous992707535
1200103734200103735CA25GENIChomozygous992707536
1200103869200103870CT16GENIChomozygous992707537
1200104376200104377GA22GENICpossibly homozygous992707538
1200104465200104466CT37GENICpossibly homozygous992707539
1200107146200107147GA23GENIChomozygous992707540
1200109793200109794TG11GENIChomozygous992707541
1200110326200110327CA34GENICpossibly homozygous992707542
1200110633200110634CT36GENIChomozygous992707543
1200110639200110640GA36GENIChomozygous992707544
1200111928200111929TC33GENICpossibly homozygous992707545
1200112480200112481AG30GENICpossibly homozygous992707546
1200112530200112531TG28GENIChomozygous992707547
1200112640200112641GA20GENICpossibly homozygous992707548
1200112829200112830AG21GENIChomozygous992707549
1200113422200113423TA22GENIChomozygous992707550
1200113468200113469CT34GENIChomozygous992707551
1200115478200115479TC33GENIChomozygous992707552