chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
167596834475968345GA49GENIChomozygous112116552
167596870775968708CT71GENIChomozygous112116554
167597148475971485CA59GENIChomozygous112116556
167597170975971710GA43GENIChomozygous112116558
167597243975972440AT45GENIChomozygous112116560
167597280075972801GA42GENIChomozygous112116562
167597294175972942TC51GENIChomozygous111864154
167597339375973397AAAC14GENICheterozygous133581261
167597463375974634GA42GENIChomozygous111864155
167597696875976969GT56GENIChomozygous112116564
167597824575978246CT41GENIChomozygous112116566
167597982975979830CT44GENICpossibly homozygous111864158
167598021875980219GA46GENIChomozygous112116568
167598192975981930AG31GENIChomozygous111864159
167598261375982614CT41GENIChomozygous112116570
167598435475984355AT49GENIChomozygous111864160
167598801075988011CT56GENIChomozygous112116572
167598816675988167GA42GENIChomozygous112116574
167597627375976273C34GENIChomozygous131182106
167598119775981198TC45GENIChomozygous112235509
167598648375986484TG23GENIChomozygous112259742
167599408275994083CT46GENIChomozygous112116576
167599773575997736TC56GENIChomozygous111864171
167600491376004914GA55GENIChomozygous111864182
167600546076005461AG54GENIChomozygous111864183
167600555176005552TC47GENIChomozygous111864184
167600577376005774AG65GENIChomozygous111864185
167600608076006081CT71GENIChomozygous112116578
167600630276006303TC42GENIChomozygous111864187
167600638676006387GA28GENIChomozygous111864188
167601325276013253GA8GENIChomozygous125693349
167601333276013333GA7GENIChomozygous125671851
167601481476014815CG41GENIChomozygous111864207
167597638675976386G43GENIChomozygous129383083
167598812975988130C54GENIChomozygous131182107
167599289475992901ACTGGAT43GENIChomozygous129383087
167601181976011819C42GENIChomozygous131182108
167601288376012883CACTCAGCTTAGCTCATGGG9GENIChomozygous132208015
167601594176015941TGT41GENIChomozygous129383094