chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
176631024366310244CT24GENIChomozygous145039554
176631030066310301CT1GENIChomozygous145158552
176631055266310552A22GENIChomozygous145024553
176631059766310598AG17GENIChomozygous145039555
176631067666310677AG13GENIChomozygous145039556
176631069966310700AG18GENIChomozygous145039557
176631071666310717CA18GENIChomozygous145039558
176631074366310744GA22GENIChomozygous145039559
176631078166310782TA29GENIChomozygous145039560
176631078266310783AT29GENIChomozygous145039561
176631081766310817G30GENIChomozygous145024554
176631082866310828AATAAAC33GENIChomozygous145024555
176631086666310867CT34GENIChomozygous145039562
176631087266310873TC36GENIChomozygous145039563
176631087366310874GA37GENIChomozygous145039564
176631088066310881GA35GENIChomozygous145039565
176631094566310946A31GENIChomozygous145024556
176631095066310951AG31GENIChomozygous145039566
176631095166310952AG31GENIChomozygous145039567
176631099266310992C32GENIChomozygous145024557
176631103466311035CT41GENIChomozygous145039568
176631103966311040TC40GENIChomozygous145039569
176631111466311115GT43GENIChomozygous145039570
176631199466311995TA50GENIChomozygous145039571
176631220466312208TCTC31GENIChomozygous145024558
176631226466312265TA28GENICpossibly homozygous145039572
176631226866312268A26GENICpossibly homozygous145024559
176631227066312271TA26GENIChomozygous145039573
176631254666312547CT55GENIChomozygous145039574
176631278366312784GA46GENICpossibly homozygous145039575
176631333766313338GA49GENICpossibly homozygous145039576
176631361466313615CT46GENIChomozygous145039577
176631377766313778GT31GENICpossibly homozygous145039578
176631382366313824TC41GENIChomozygous145039579
176631428866314289CT55GENICpossibly homozygous145039580
176631524766315248GC43GENIChomozygous145039581
176631230066312300A26GENIChomozygous140033418
176631184866311849AG43GENIChomozygous140165594
176631413566314136GA45GENIChomozygous140165596