chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4155682235155682236C14GENIChomozygous128094660
4155682479155682479TT17GENIChomozygous128094661
4155682881155682882TG10GENIChomozygous112896524
4155683727155683728GA14GENIChomozygous112896526
4155686203155686203C8GENICheterozygous128094662
4155686300155686301AC10GENIChomozygous112896528
4155686301155686302AG10GENIChomozygous112896530
4155686396155686397TG14GENIChomozygous112896532
4155686780155686781GC3GENIChomozygous112896534
4155686827155686827C4GENIChomozygous128094663
4155686834155686834A4GENIChomozygous128094664
4155686907155686907A7GENIChomozygous128094665
4155686943155686943C8GENIChomozygous128094666
4155686959155686960GA8GENIChomozygous112896536
4155687362155687363TA7GENIChomozygous112896538
4155687387155687388GA8GENIChomozygous112896540
4155687673155687674GA18GENIChomozygous112896542
4155689066155689067GA19GENIChomozygous112896546
4155689093155689094CG21GENIChomozygous112896548
4155689531155689532CT19GENIChomozygous112896550
4155690256155690257AC17GENIChomozygous112896552
4155690460155690460A15GENIChomozygous128094670
4155686203155686204TC8GENICheterozygous128137163
4155686967155686967A8GENIChomozygous128094667
4155688889155688889T25GENICheterozygous128094668
4155688906155688910ATTT21GENICheterozygous128094669