chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109121234391212351GTGTGTGT--------7GENICpossibly homozygous52508753
109121286691212867CA15GENIChomozygous51539279
109121323491213235CG32GENIChomozygous52166056
109121580691215807C-17GENIChomozygous51539280
109121584891215858GTGTGTGTGT----------6GENICheterozygous51539281
109121636091216361GA40GENIChomozygous51539282
109121671291216713CT22GENIChomozygous51539283
109121698291216983GC14GENIChomozygous52166057
109121775791217758AG22GENIChomozygous52166058
109121793791217938C-33GENIChomozygous51739178
109121796491217965CT36GENIChomozygous51739180
109121811491218115G-22INTERGENICpossibly homozygous51739182
109121814691218150TCTT----33INTERGENIChomozygous52166059
109121968791219688GT14GENIChomozygous51539284
109121975891219759AATCTGAGGCC20GENIChomozygous52166060
109122028991220290GA31GENIChomozygous52166061
109122045291220453AG31GENIChomozygous51739188
109122071491220715TC28GENIChomozygous52166062
109122075391220754AT30GENIChomozygous51539287
109122108491221085GA33GENIChomozygous51539288
109122121891221226CTTTTTTT--------27GENIChomozygous51539289
109122129491221295CT18GENIChomozygous52166063
109122147791221478CG25GENIChomozygous51539293
109122158091221581CT26GENIChomozygous51539294
109122163491221635AG41GENIChomozygous51539295
109122213291222133GA28GENIChomozygous51539296