chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4155682235155682236C21GENIChomozygous128094660
4155682479155682479TT20GENIChomozygous128094661
4155682881155682882TG15GENIChomozygous112896524
4155683727155683728GA32GENIChomozygous112896526
4155686203155686204TC21GENICheterozygous128137163
4155686203155686203C21GENICheterozygous128094662
4155686300155686301AC20GENIChomozygous112896528
4155686301155686302AG20GENIChomozygous112896530
4155686396155686397TG14GENIChomozygous112896532
4155686780155686781GC10GENIChomozygous112896534
4155686827155686827C11GENIChomozygous128094663
4155686834155686834A11GENIChomozygous128094664
4155686907155686907A11GENIChomozygous128094665
4155686943155686943C9GENIChomozygous128094666
4155686959155686960GA12GENIChomozygous112896536
4155686967155686967A13GENIChomozygous128094667
4155687362155687363TA15GENIChomozygous112896538
4155687387155687388GA17GENIChomozygous112896540
4155687673155687674GA18GENIChomozygous112896542
4155688889155688889T35GENICheterozygous128094668
4155688906155688910ATTT28GENICheterozygous128094669
4155689066155689067GA18GENIChomozygous112896546
4155689093155689094CG16GENIChomozygous112896548
4155689531155689532CT18GENIChomozygous112896550
4155690256155690257AC22GENIChomozygous112896552
4155690460155690460A22GENICpossibly homozygous128094670