chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
167486558474865585GA23GENICpossibly homozygous111861998
167486575674865757TC24GENICpossibly homozygous111861999
167486576874865769TC25GENICpossibly homozygous111862000
167486577774865778TG23GENICpossibly homozygous111862001
167486601574866016CT20GENIChomozygous111862002
167486685174866852AG23GENICpossibly homozygous111862003
167486686774866868CT28GENICpossibly homozygous111862004
167486809874868099TG34GENICpossibly homozygous111862005
167487016574870166GA30GENICpossibly homozygous112323929
167487020274870203CT25GENIChomozygous112323930
167487075674870757AT26GENICpossibly homozygous111862010
167487906574879066CT30GENICpossibly homozygous112132620
167487909774879098AG29GENICpossibly homozygous112132622
167487917874879179CT20GENICpossibly homozygous112323931
167487964374879644GT4GENIChomozygous111862021
167487967874879679AT3GENIChomozygous111862022
167487967974879680TG3GENIChomozygous111862023
167487974074879741TC11GENIChomozygous111862024
167487985574879856CG8GENIChomozygous111862025
167488004974880050GC12GENIChomozygous112115790
167488013174880132AG23GENIChomozygous111862026
167488015974880160CG26GENIChomozygous111862027
167488022574880226GA26GENICpossibly homozygous111862028
167488132674881327TG21GENIChomozygous112115794
167488277274882773CT30GENICpossibly homozygous112361772
167488306774883068TC22GENICpossibly homozygous111862034
167488459474884595CT19GENICpossibly homozygous112323940
167488459974884600AG17GENICpossibly homozygous111862037
167488472674884727TC21GENICpossibly homozygous111862038
167488525374885254AG32GENICpossibly homozygous111862040
167488531774885318CT36GENIChomozygous112323941
167488563374885634CT12GENIChomozygous111862041
167488567274885673CT19GENIChomozygous112323942
167488573874885739TC25GENIChomozygous112323943
167488665774886658CT23GENIChomozygous112323944
167489001174890012CT20GENIChomozygous112361776