chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7121890038121890038A29GENIChomozygous128513134
7121890041121890041C29GENIChomozygous128513135
7121890045121890046C29GENIChomozygous128513136
7121890057121890058T28GENIChomozygous128513137
7121890063121890064T28GENIChomozygous128513138
7121890068121890068T28GENIChomozygous128513139
7121890079121890080G26GENIChomozygous128513140
7121890091121890091CA24GENIChomozygous128513141
7121890100121890101GT24GENIChomozygous115860197
7121890105121890105C22GENIChomozygous128513142
7121890117121890118A21GENIChomozygous128513143
7121890138121890139A22GENIChomozygous128513144
7121890156121890157A25GENIChomozygous128513145
7121890160121890160T27GENIChomozygous128513146
7121890178121890178T26GENIChomozygous128513147
7121890180121890181CG27GENIChomozygous116225629
7121890184121890185G28GENIChomozygous128513148
7121890190121890190C30GENIChomozygous128513149
7121890220121890221TA36GENIChomozygous118360376
7121890221121890222AT36GENIChomozygous118360378
7121890226121890227GA34GENIChomozygous116082029
7121890232121890233G33GENIChomozygous128513150
7121890238121890238T33GENIChomozygous128513151
7121890241121890242T33GENIChomozygous128513152
7121890262121890263TC40GENIChomozygous115860199
7121890267121890267A40GENIChomozygous128513153
7121891770121891770G47GENIChomozygous128513154
7121900476121900476A46GENIChomozygous128513156
7121900477121900478TA47GENIChomozygous118259194
7121900486121900487G46GENIChomozygous128513157
7121900516121900517CT49GENIChomozygous115860201
7121900542121900543G48GENIChomozygous128513158
7121900556121900557T47GENIChomozygous128513159
7121900567121900568G47GENIChomozygous128513160
7121905390121905392TG42GENICheterozygous128513161
7121912799121912799A37GENICpossibly homozygous128513162
7121915601121915602G57GENIChomozygous128513163
7121915605121915606GT57GENIChomozygous118259196
7121915618121915619T54GENIChomozygous128513164
7121915625121915626CA55GENIChomozygous115860203
7121915626121915627AC54GENIChomozygous115860205