chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1240372812240372813TG21GENIChomozygous108588285
1240372930240372931CT19GENIChomozygous109540010
1240373242240373243GA20GENIChomozygous109540011
1240373466240373467AG22GENIChomozygous109540012
1240373474240373475AG22GENIChomozygous109540013
1240373762240373763AT31GENIChomozygous108588286
1240374073240374074CT17GENIChomozygous109540014
1240374382240374383TA23GENIChomozygous109540015
1240374439240374440GA29GENIChomozygous109540016
1240374554240374555GT23GENIChomozygous109540017
1240375380240375381CT27GENIChomozygous109540018
1240375392240375393TC24GENIChomozygous109540019
1240375456240375457CT25GENIChomozygous109540020
1240375894240375895TC20GENIChomozygous108588289
1240376026240376027AG20GENIChomozygous109540021
1240376075240376076CT27GENIChomozygous109540022
1240376174240376175GA17GENIChomozygous109540023
1240376225240376226TC20GENIChomozygous109540024
1240376662240376663CG37GENIChomozygous108588292
1240376751240376752AG39GENIChomozygous109540025
1240377360240377361GA35GENICpossibly homozygous108588294
1240377416240377417CT30GENIChomozygous108588295
1240378064240378065CA42GENIChomozygous108588296