chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10104053280104053280G47GENIChomozygous128855578
10104053824104053824G38GENIChomozygous128855579
10104053836104053837A40GENIChomozygous128855580
10104053840104053840G39GENIChomozygous128855581
10104053845104053846TC40GENIChomozygous116713700
10104053883104053883G25GENIChomozygous128855582
10104053899104053900C23GENIChomozygous128855583
10104053917104053918C15GENIChomozygous128855584
10104053924104053924G10GENIChomozygous128855585
10104053927104053931AAAG8GENIChomozygous128855586
10104053935104053936A7GENIChomozygous128855587
10104053939104053940A6GENIChomozygous128855588
10104053955104053958AGA6GENIChomozygous128855589
10104053961104053962T12GENIChomozygous128855590
10104053964104053964G12GENIChomozygous128855591
10104053980104053980T14GENIChomozygous128855592
10104053991104053992CA15GENIChomozygous128874883
10104053949104053950AG6GENIChomozygous128874880
10104053951104053952AG6GENIChomozygous128874881
10104053988104053989AT16GENIChomozygous128874882
10104053992104053993AG14GENIChomozygous128874884
10104053995104053998AAC14GENIChomozygous128855593
10104053999104053999C14GENIChomozygous128855594
10104054026104054028AG16GENIChomozygous128855595
10104054034104054035G16GENIChomozygous128855596
10104054035104054036GT16GENIChomozygous123417428
10104054044104054045T16GENIChomozygous128855597
10104054050104054051G16GENIChomozygous128855598
10104054054104054055G16GENIChomozygous128855599
10104054068104054069T15GENIChomozygous128855600
10104054072104054072CGCGC14GENIChomozygous128855601
10104054075104054076G14GENIChomozygous128855602
10104054088104054088C13GENIChomozygous128855603
10104054101104054102A9GENIChomozygous128855604
10104054132104054133G4GENIChomozygous132881933