chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106170490261704903GT27GENIChomozygous116790687
106170609861706099AG36GENIChomozygous116939449
106170738261707383AG39GENIChomozygous116613020
106170897961708980TC34GENIChomozygous116613024
106170904761709048TC41GENIChomozygous116613026
106170938061709381TA22GENIChomozygous116613028
106171149861711499GT24GENIChomozygous116613032
106171152561711526AT23GENIChomozygous116613034
106171191861711919CA27GENIChomozygous116613036
106171213061712131AC25GENIChomozygous116613038
106171324761713248TC31GENIChomozygous116613040
106171404261714043GA29GENICpossibly homozygous116790689
106171408961714090CT35GENIChomozygous116790691
106171501961715020AG35GENIChomozygous116790693
106172113161721132TC32GENIChomozygous117012806
106172422361724224CA35GENIChomozygous116790695
106172669361726694CG32GENIChomozygous116790697
106172673661726737GC34GENIChomozygous116613045
106173106561731066CT33GENIChomozygous116790699
106173223761732238CG28GENIChomozygous116613047
106173309361733094AT12GENIChomozygous116790701
106173567161735672CG40GENIChomozygous117012807
106173574961735750GA27GENIChomozygous116790707
106174196261741963CT21GENIChomozygous116790711
106174230361742304TC42GENIChomozygous116790713
106174475261744753AC24GENIChomozygous117061705
106172269961722700CG10GENIChomozygous117196191