chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134790630447906305GA13GENIChomozygous114548465
134790858447908585AT23GENIChomozygous114548467
134790903547909036CT13GENIChomozygous114548468
134790985047909851GA30GENIChomozygous114548469
134791039647910397AG20GENIChomozygous114548470
134791053247910533CT25GENIChomozygous114548471
134791124547911246TC31GENIChomozygous114548472
134791150447911505CT23GENIChomozygous114548473
134791183147911832CT29GENIChomozygous114548474
134791280047912801AG20GENIChomozygous114548475
134791284247912843CT19GENIChomozygous114548476
134791303847913039CA20GENICpossibly homozygous114548477
134791317347913174CT15GENIChomozygous114548478
134791460047914601TG8GENICheterozygous114548479
134791474747914748TA12GENIChomozygous114548480
134791481247914813CT12GENIChomozygous114548481
134791440947914410GA18GENIChomozygous114760408
134791508247915083AG9GENIChomozygous114548482
134791583147915832GA27GENIChomozygous114548483
134791631047916311GC19GENIChomozygous114871690
134791653747916538TG10GENIChomozygous114720022
134791618447916185GT25GENIChomozygous114337866