chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
107006970970069710GT17GENIChomozygous117368899
107006979770069798AG16GENIChomozygous117151739
107008152370081533TTTCTTTCTT19GENIChomozygous135201906
107008155970081559G15GENICpossibly homozygous128828797
107009402070094021TC22GENICheterozygous128871096
107009411670094117AG12GENICheterozygous128871098
107010114270101143TC23GENICheterozygous117999818
107010114670101147GA22GENICheterozygous118042666
107010121670101217GA24GENICheterozygous123380290
107010121770101218CT25GENICheterozygous123380291
107010121870101219GT25GENICheterozygous123380292
107010122170101222AG24GENICheterozygous118084289
107010123170101232CA24GENICheterozygous117999819
107010125370101254AC34GENICheterozygous117999820
107010127070101271TC37GENICheterozygous117999821
107010127670101277GA39GENICheterozygous117999822
107010128070101281TC38GENICheterozygous117312913
107010135070101351GA35GENICheterozygous116627085
107010540770105408AT7GENIChomozygous116627097
107010770570107705A19GENIChomozygous135201907
107011089470110894TTTTA16GENIChomozygous128828814
107011615870116159CA16GENIChomozygous117368901
107011763070117631AG29GENIChomozygous116627147