chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4155682235155682236C23GENIChomozygous128094660
4155682479155682479TT13GENIChomozygous128094661
4155682881155682882TG14GENIChomozygous112896524
4155683727155683728GA21GENIChomozygous112896526
4155686203155686203C19GENIChomozygous128094662
4155686300155686301AC10GENIChomozygous112896528
4155686301155686302AG10GENIChomozygous112896530
4155686396155686397TG15GENIChomozygous112896532
4155686780155686781GC6GENIChomozygous112896534
4155686827155686827C4GENIChomozygous128094663
4155686834155686834A4GENIChomozygous128094664
4155686907155686907A4GENIChomozygous128094665
4155686943155686943C6GENIChomozygous128094666
4155686959155686960GA7GENIChomozygous112896536
4155686967155686967A5GENIChomozygous128094667
4155687362155687363TA16GENIChomozygous112896538
4155687387155687388GA14GENIChomozygous112896540
4155687673155687674GA21GENIChomozygous112896542
4155688889155688889T25GENICheterozygous128094668
4155688906155688910ATTT22GENICheterozygous128094669
4155689066155689067GA17GENIChomozygous112896546
4155689093155689094CG18GENIChomozygous112896548
4155689531155689532CT13GENIChomozygous112896550
4155690256155690257AC20GENIChomozygous112896552
4155690460155690460A21GENIChomozygous128094670