chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1265321114265321115AG20GENIChomozygous108636955
1265325653265325654GA27GENIChomozygous108636958
1265326562265326563AC26GENIChomozygous108636959
1265329955265329956AG36GENIChomozygous108636960
1265332084265332085CA39GENIChomozygous108636961
1265332161265332162TC30GENIChomozygous108636962
1265332199265332200GA28GENIChomozygous108636963
1265332319265332320GA25GENIChomozygous108636964
1265333578265333579CT29GENIChomozygous108636967
1265335735265335736CT34GENIChomozygous108636968
1265336933265336934TC26GENIChomozygous108636969
1265337926265337927AG27GENIChomozygous108636970
1265338261265338262CT26GENIChomozygous108636972
1265342019265342020CT18GENIChomozygous108636978
1265342021265342022CT17GENIChomozygous108636979
1265344537265344538AC23GENIChomozygous108636983
1265345093265345094AC44GENIChomozygous108636984
1265345313265345314AG25GENIChomozygous108636985
1265346066265346067AG26GENIChomozygous108636986
1265346791265346792GA19GENIChomozygous108636987
1265346889265346890AC22GENIChomozygous108636988
1265347349265347350CA32GENIChomozygous108636989
1265347455265347456TC36GENIChomozygous108636990
1265348252265348253GA17GENIChomozygous108636991
1265354610265354611TC31GENIChomozygous108636992
1265357351265357352AT22GENIChomozygous108637007
1265357401265357402CT24GENIChomozygous108637008
1265358365265358366CT21GENICpossibly homozygous108637009
1265362451265362452GA28GENIChomozygous108637010
1265365439265365440GA24GENIChomozygous108637014
1265365451265365452GA29GENIChomozygous108637015
1265368281265368282TC15GENIChomozygous108637016
1265372764265372765GA12GENIChomozygous108637017
1265338521265338522AT20GENIChomozygous109218242
1265341428265341429CT21GENIChomozygous120477283
1265342017265342018CT14GENICpossibly homozygous120477284