chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
17400985874009859AG16GENIChomozygous109292872
17401283974012840AC24GENICheterozygous109292873
17401973474019735GA5GENICheterozygous109292874
17402003874020039AT36GENICheterozygous109292875
17402046274020463CT40GENICheterozygous109292876
17402170374021704GT33GENICpossibly homozygous109292877
17402243774022438GT62GENICheterozygous109292878
17402299674022997CA21GENICpossibly homozygous109292879
17402311574023116AG47GENICheterozygous109292880
17402317674023177GT69GENICheterozygous109292881
17402336174023362AG247GENICheterozygous109292882
17402347774023478GA250GENICheterozygous108133814
17402349274023493AT250GENICheterozygous108133815
17401214874012149TC21GENIChomozygous108868086
17401269274012693GT20GENIChomozygous108868087
17402478174024782GA12GENIChomozygous108133816
17402478574024786AG11GENIChomozygous108133817
17402478974024790GA10GENIChomozygous108133818
17402490674024907AT19GENIChomozygous108133819
17402490874024909AT18GENIChomozygous108133820
17402490974024910AC18GENIChomozygous108133821
17402512974025130GA26GENICpossibly homozygous109292883
17402518474025185GC29GENICheterozygous109292884
17402581874025819AC22GENIChomozygous109292885
17402582874025829TA23GENIChomozygous109292886
17402633474026335GC11GENIChomozygous109292887
17402657174026572AC18GENIChomozygous109292888
17402905974029060CG21GENIChomozygous109292889
17402919974029200AT26GENIChomozygous108868097
17402947574029476AG35GENIChomozygous108868099