chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1164803991164803992CT70INTERGENIChomozygous60925979
1164804016164804017TC69INTERGENICpossibly homozygous60925980
1164804080164804081AG58INTERGENIChomozygous60925981
1164804109164804110GC67INTERGENIChomozygous60925982
1164804469164804470TC48INTERGENIChomozygous60925983
1164805359164805360TG94INTERGENICpossibly homozygous60925984
1164805509164805510GGA64INTERGENIChomozygous60925985
1164805561164805562AG63INTERGENICpossibly homozygous60925986
1164805664164805665CT55INTERGENIChomozygous60925987
1164805673164805674CT57INTERGENIChomozygous60925988
1164805707164805708CG62INTERGENIChomozygous60925989
1164805755164805756AC53INTERGENIChomozygous60925990
1164805913164805914T-44INTERGENIChomozygous60925991
1164805952164805953TG49INTERGENICpossibly homozygous60925992
1164805956164805957AG47INTERGENICpossibly homozygous60925993
1164806580164806581GC35INTERGENIChomozygous60925994
1164806899164806907ATATATAC--------43INTERGENIChomozygous60925996
1164807740164807741AG12INTERGENICheterozygous60925997
1164807742164807743AG12INTERGENICheterozygous61308866
1164807966164807967AC78INTERGENIChomozygous60925998
1164808087164808088TTG64INTERGENIChomozygous60925999
1164808324164808325AG60INTERGENIChomozygous60926000
1164808764164808766AA--48INTERGENIChomozygous60926001
1164808845164808846TA51INTERGENIChomozygous60926002
1164809096164809097AG42INTERGENIChomozygous60926003
1164809889164809890TC46INTERGENIChomozygous60926004
1164809893164809894TC48INTERGENIChomozygous60926005
1164809911164809912CT46INTERGENIChomozygous60926006
1164810057164810058TC62INTERGENIChomozygous60926007
1164810130164810131CCTT33INTERGENIChomozygous60926008
1164810740164810741GC41INTERGENICheterozygous60926009
1164810740164810741GGTGTC19INTERGENICheterozygous60926010
1164810740164810741GGTC19INTERGENICheterozygous60926011
1164810757164810761TGTC----27INTERGENICheterozygous60926012
1164810768164810769GC39INTERGENICpossibly homozygous60926013