chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104678683446786835TC18GENIChomozygous116586642
104678757646787577CT37GENIChomozygous116586644
104678784246787843CT27GENIChomozygous116586646
104678799146787992TC11GENIChomozygous116586648
104678965546789656GA16GENIChomozygous116586650
104678973746789738TC15GENIChomozygous116586652
104679023246790233CT20GENIChomozygous116586654
104679104246791043TA27GENIChomozygous116586656
104679104846791049AG28GENIChomozygous116586658
104679126846791269CT18GENIChomozygous116586660
104679194146791942TA25GENIChomozygous116586664
104679200946792010TC27GENIChomozygous116586666
104679214546792146CT16GENIChomozygous116586668
104679297746792978CT30GENIChomozygous116586670
104679301446793015CG23GENIChomozygous116586672
104679392146793922CT23GENIChomozygous116877970
104679507046795071AG11GENIChomozygous116586674
104679649046796491AT24GENIChomozygous116586678
104679937146799372GA20GENIChomozygous116586682
104680138246801383GT31GENICpossibly homozygous116586684
104680139146801392AG32GENIChomozygous116586686
104680203246802033GC25GENIChomozygous116586688
104680313046803131CG24GENIChomozygous116586690
104680407346804074GA25GENIChomozygous116586695
104680603246806033CT40GENIChomozygous116586699
104680713246807133TC33GENIChomozygous116586701
104680798846807989CT19GENIChomozygous116586703
104680839146808392TC12GENIChomozygous116586705
104680839546808396GA12GENIChomozygous116586707
104680895946808960AG26GENIChomozygous116586709
104680928446809285TC17GENIChomozygous116586711
104680933546809336CA23GENIChomozygous116586713
104679292646792927GA27GENIChomozygous117252983
104680272746802728TC34GENIChomozygous117252985
104680315446803155TC22GENIChomozygous117252987
104680669046806691TC23GENIChomozygous116931556