chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18242483482424835AG21GENIChomozygous108878096
18242600182426002AG32GENIChomozygous108878097
18242758182427582TC20GENIChomozygous108878099
18242771082427711CT26GENIChomozygous108878100
18242873982428740CT23GENIChomozygous108878101
18242891282428913AG30GENIChomozygous120481877
18242940882429409CT33GENIChomozygous108878102
18243036282430363TG27GENIChomozygous108878103
18243283182432832AC23GENIChomozygous108878105
18243285082432851GA24GENIChomozygous120559008
18243681882436819CT40GENIChomozygous108878114
18243688282436883GC12GENIChomozygous108878115
18243779982437800TC28GENIChomozygous108878116
18243818582438186GA36GENIChomozygous109302466
18243857882438579AG27GENIChomozygous108878117
18244047882440479GA33GENIChomozygous120559010
18244264082442641CT26GENIChomozygous120559012
18244286082442861CT43GENIChomozygous120559014
18244309682443097TC30GENIChomozygous120559016
18244499682444997CT36GENIChomozygous109302474
18244549282445493TC29GENIChomozygous108878132
18244572282445723CT33GENIChomozygous109302476
18244785582447856GC43GENIChomozygous108878148
18244808082448081AG34GENIChomozygous108878149
18244810982448110CT33GENIChomozygous108878150
18244821882448219CT36GENIChomozygous108878151
18244824382448244TG32GENIChomozygous108878152
18244863882448639GA39GENIChomozygous120559018
18244903182449032GA26GENIChomozygous120559020
18244969882449699CA23GENIChomozygous108878155
18244971182449712AC25GENIChomozygous108878156
18245120582451206GA25GENIChomozygous120559022
18245179482451795CT43GENIChomozygous108878158
18245186282451863GA25GENIChomozygous120559024