chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1240372812240372813TG20GENIChomozygous108588285
1240372930240372931CT18GENIChomozygous109540010
1240373242240373243GA11GENIChomozygous109540011
1240373466240373467AG21GENIChomozygous109540012
1240373474240373475AG21GENIChomozygous109540013
1240373762240373763AT21GENIChomozygous108588286
1240374073240374074CT10GENIChomozygous109540014
1240374382240374383TA23GENIChomozygous109540015
1240374554240374555GT8GENIChomozygous109540017
1240375380240375381CT11GENIChomozygous109540018
1240375392240375393TC12GENIChomozygous109540019
1240375456240375457CT16GENIChomozygous109540020
1240375894240375895TC13GENIChomozygous108588289
1240376026240376027AG17GENIChomozygous109540021
1240376075240376076CT14GENIChomozygous109540022
1240376174240376175GA30GENIChomozygous109540023
1240376225240376226TC30GENIChomozygous109540024
1240376351240376352TC24GENIChomozygous108588291
1240376662240376663CG26GENIChomozygous108588292
1240376751240376752AG39GENIChomozygous109540025
1240377360240377361GA26GENIChomozygous108588294
1240377416240377417CT23GENIChomozygous108588295
1240378064240378065CA20GENIChomozygous108588296