chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117042314117042315GT45GENIChomozygous115846155
7117043615117043616TC37GENIChomozygous115846157
7117046238117046239TG30GENIChomozygous115846159
7117046634117046635TG33GENIChomozygous115846175
7117046642117046643GC32GENIChomozygous115846177
7117046643117046644TA32GENIChomozygous115846179
7117048001117048002TC33GENIChomozygous115846181
7117048750117048751GA23GENIChomozygous115846183
7117049548117049549A32GENIChomozygous128510433
7117049276117049278TC28GENICpossibly homozygous128510432
7117046278117046279A28GENIChomozygous128510429
7117048325117048325A17GENICheterozygous128510431
7117050030117050032TA34GENIChomozygous128510434
7117050309117050310TC39GENIChomozygous115846185
7117050544117050545AG37GENIChomozygous115846187
7117051060117051061A34GENIChomozygous128510435
7117051084117051085GA36GENIChomozygous115846189
7117051518117051519CT59GENICheterozygous115846191
7117051731117051732GA64GENIChomozygous115846193
7117051766117051766AT53GENICheterozygous128510436
7117052103117052104GA52GENIChomozygous115846195
7117052654117052654AGAGA30GENIChomozygous128510438
7117053228117053229GA35GENIChomozygous115846197
7117053322117053323CT39GENIChomozygous115846199
7117053942117053942C30GENIChomozygous128510439
7117054348117054349AG19GENIChomozygous115846201
7117054379117054380GT19GENIChomozygous116301967
7117054380117054381GT19GENIChomozygous118258905
7117054480117054481G31GENIChomozygous128510440
7117058574117058575GA36GENIChomozygous115846203
7117061618117061619GA43GENIChomozygous115846205
7117051271117051272AG38GENICheterozygous128562334
7117051406117051407AT49GENICheterozygous116224751