chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1164803991164803992CT28INTERGENIChomozygous60925979
1164804016164804017TC22INTERGENIChomozygous60925980
1164804080164804081AG26INTERGENIChomozygous60925981
1164804109164804110GC30INTERGENIChomozygous60925982
1164804469164804470TC28INTERGENIChomozygous60925983
1164805359164805360TG16INTERGENIChomozygous60925984
1164805509164805510GGA11INTERGENIChomozygous60925985
1164805561164805562AG9INTERGENIChomozygous60925986
1164805664164805665CT15INTERGENIChomozygous60925987
1164805673164805674CT17INTERGENIChomozygous60925988
1164805707164805708CG16INTERGENIChomozygous60925989
1164805755164805756AC23INTERGENIChomozygous60925990
1164805913164805914T-23INTERGENIChomozygous60925991
1164805952164805953TG22INTERGENIChomozygous60925992
1164805956164805957AG23INTERGENIChomozygous60925993
1164806580164806581GC14INTERGENIChomozygous60925994
1164806899164806907ATATATAC--------1INTERGENIChomozygous60925996
1164807694164807695GA1INTERGENIChomozygous62247333
1164807696164807697GA1INTERGENIChomozygous62247334
1164807698164807699GA2INTERGENIChomozygous62247335
1164807742164807743AATGTGTGTG3INTERGENIChomozygous62247336
1164807966164807967AC14INTERGENIChomozygous60925998
1164808087164808088TTG18INTERGENIChomozygous60925999
1164808324164808325AG22INTERGENIChomozygous60926000
1164808764164808766AA--17INTERGENIChomozygous60926001
1164808845164808846TA23INTERGENIChomozygous60926002
1164809096164809097AG7INTERGENIChomozygous60926003
1164809889164809890TC20INTERGENIChomozygous60926004
1164809893164809894TC21INTERGENIChomozygous60926005
1164809911164809912CT22INTERGENIChomozygous60926006
1164810057164810058TC24INTERGENIChomozygous60926007
1164810130164810131CCTT18INTERGENICpossibly homozygous60926008
1164810130164810131CCT18INTERGENICheterozygous61777234
1164810740164810741GGTGTC10INTERGENICheterozygous60926010
1164810740164810741GGTC10INTERGENICheterozygous60926011
1164810768164810769GC30INTERGENIChomozygous60926013