chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4155682235155682236C44GENIChomozygous128094660
4155682479155682479TT41GENIChomozygous128094661
4155682881155682882TG45GENICpossibly homozygous112896524
4155686300155686301AC29GENIChomozygous112896528
4155686301155686302AG29GENIChomozygous112896530
4155686396155686397TG28GENIChomozygous112896532
4155686780155686781GC22GENIChomozygous112896534
4155686834155686834A19GENIChomozygous128094664
4155686907155686907A17GENIChomozygous128094665
4155686943155686943C16GENIChomozygous128094666
4155686959155686960GA24GENIChomozygous112896536
4155686967155686967A25GENICpossibly homozygous128094667
4155687362155687363TA47GENIChomozygous112896538
4155687387155687388GA48GENIChomozygous112896540
4155687673155687674GA36GENIChomozygous112896542
4155688889155688889T26GENICheterozygous128094668
4155688906155688910ATTT30GENIChomozygous128094669
4155689093155689094CG35GENIChomozygous112896548
4155689531155689532CT29GENIChomozygous112896550
4155690460155690460A46GENICpossibly homozygous128094670
4155686830155686830T20GENIChomozygous130939443
4155691113155691114T37GENIChomozygous130939444