chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1164803991164803992CT14INTERGENIChomozygous60925979
1164804016164804017TC12INTERGENIChomozygous60925980
1164804080164804081AG22INTERGENIChomozygous60925981
1164804109164804110GC23INTERGENIChomozygous60925982
1164804469164804470TC13INTERGENIChomozygous60925983
1164805359164805360TG11INTERGENIChomozygous60925984
1164805509164805510GGA28INTERGENIChomozygous60925985
1164805561164805562AG26INTERGENIChomozygous60925986
1164805664164805665CT19INTERGENIChomozygous60925987
1164805673164805674CT18INTERGENIChomozygous60925988
1164805707164805708CG20INTERGENIChomozygous60925989
1164805755164805756AC22INTERGENIChomozygous60925990
1164805913164805914T-17INTERGENIChomozygous60925991
1164805952164805953TG21INTERGENIChomozygous60925992
1164805956164805957AG25INTERGENIChomozygous60925993
1164806580164806581GC27INTERGENIChomozygous60925994
1164806877164806893ATATATATATATACAT----------------8INTERGENICheterozygous60925995
1164806899164806907ATATATAC--------10INTERGENIChomozygous60925996
1164807740164807741AG9INTERGENICheterozygous60925997
1164807742164807743AG10INTERGENICheterozygous61308866
1164807966164807967AC19INTERGENIChomozygous60925998
1164808087164808088TTG25INTERGENIChomozygous60925999
1164808324164808325AG32INTERGENIChomozygous60926000
1164808764164808766AA--22INTERGENIChomozygous60926001
1164808845164808846TA16INTERGENIChomozygous60926002
1164809096164809097AG8INTERGENIChomozygous60926003
1164809889164809890TC24INTERGENIChomozygous60926004
1164809893164809894TC24INTERGENIChomozygous60926005
1164809911164809912CT27INTERGENIChomozygous60926006
1164810057164810058TC27INTERGENIChomozygous60926007
1164810130164810131CCTT19INTERGENIChomozygous60926008
1164810740164810741GC38INTERGENICheterozygous60926009
1164810740164810741GGTGTC23INTERGENICpossibly homozygous60926010
1164810740164810741GGTC23INTERGENICheterozygous60926011
1164810768164810769GC31INTERGENICpossibly homozygous60926013