chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6110968339110968340AG33GENIChomozygous114940146
6110968390110968391CG30GENIChomozygous114940147
6110968791110968792AC34GENIChomozygous115276443
6110971410110971411GT11GENIChomozygous115276445
6110971782110971783CT19GENIChomozygous115276447
6110973238110973239CT13GENIChomozygous114940153
6110973277110973278AT22GENICpossibly homozygous114940154
6110973593110973594GT12GENIChomozygous114940155
6110973745110973746GT20GENIChomozygous114940156
6110978397110978398GC6GENIChomozygous114940158
6110981050110981051AG30GENIChomozygous114940162
6110982217110982218GT24GENIChomozygous114940164
6110982362110982363GT27GENIChomozygous114940165
6110984476110984477TG10GENIChomozygous114940166
6110985747110985748AT21GENIChomozygous115276449
6110988408110988409AG32GENIChomozygous115276451
6110988424110988425AG30GENIChomozygous115276453
6110988443110988444CT28GENIChomozygous114940169
6110988477110988478CT30GENIChomozygous114940170
6110988868110988869TC30GENIChomozygous114940171
6110988939110988940AC31GENIChomozygous114940172
6110989591110989592AT32GENIChomozygous115225477
6110989963110989964TC25GENIChomozygous114940174
6110990006110990007TC27GENIChomozygous114940175