chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1164803991164803992CT18INTERGENIChomozygous60925979
1164804016164804017TC16INTERGENICpossibly homozygous60925980
1164804080164804081AG19INTERGENIChomozygous60925981
1164804109164804110GC28INTERGENIChomozygous60925982
1164804469164804470TC13INTERGENIChomozygous60925983
1164805359164805360TG3INTERGENIChomozygous60925984
1164805561164805562AG2INTERGENIChomozygous60925986
1164805664164805665CT6INTERGENIChomozygous60925987
1164805673164805674CT6INTERGENIChomozygous60925988
1164805707164805708CG9INTERGENIChomozygous60925989
1164805755164805756AC10INTERGENIChomozygous60925990
1164805913164805914T-8INTERGENICpossibly homozygous60925991
1164805952164805953TG7INTERGENIChomozygous60925992
1164805956164805957AG8INTERGENIChomozygous60925993
1164806580164806581GC15INTERGENIChomozygous60925994
1164807966164807967AC1INTERGENIChomozygous60925998
1164808087164808088TTG8INTERGENIChomozygous60925999
1164808324164808325AG2INTERGENIChomozygous60926000
1164808619164808620GA2INTERGENICheterozygous62023903
1164808764164808766AA--1INTERGENIChomozygous60926001
1164808845164808846TA9INTERGENICpossibly homozygous60926002
1164809889164809890TC9INTERGENIChomozygous60926004
1164809893164809894TC9INTERGENIChomozygous60926005
1164809911164809912CT14INTERGENIChomozygous60926006
1164810057164810058TC19INTERGENIChomozygous60926007
1164810768164810769GC11INTERGENICheterozygous60926013