chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6110968339110968340AG33GENIChomozygous114940146
6110968390110968391CG26GENIChomozygous114940147
6110969127110969128GC25GENIChomozygous114940148
6110969169110969170GA30GENIChomozygous114940149
6110971643110971644CT30GENIChomozygous114940150
6110972161110972162TC28GENIChomozygous114940151
6110972827110972828GA24GENICpossibly homozygous114940152
6110973238110973239CT32GENIChomozygous114940153
6110973277110973278AT22GENIChomozygous114940154
6110973593110973594GT22GENIChomozygous114940155
6110973745110973746GT47GENIChomozygous114940156
6110976053110976054CT22GENIChomozygous114940157
6110978397110978398GC7GENIChomozygous114940158
6110978462110978463AG26GENIChomozygous114940159
6110978503110978504AG25GENIChomozygous114940160
6110978848110978849CT27GENIChomozygous114940161
6110981050110981051AG24GENIChomozygous114940162
6110981847110981848CT19GENIChomozygous114940163
6110982217110982218GT21GENIChomozygous114940164
6110982362110982363GT12GENIChomozygous114940165
6110984476110984477TG32GENIChomozygous114940166
6110986427110986428TG40GENIChomozygous114940167
6110987939110987940TG47GENIChomozygous114940168
6110988443110988444CT45GENIChomozygous114940169
6110988477110988478CT51GENICpossibly homozygous114940170
6110988868110988869TC30GENIChomozygous114940171
6110988939110988940AC27GENIChomozygous114940172
6110989342110989343AG16GENIChomozygous114940173
6110989963110989964TC30GENIChomozygous114940174
6110990006110990007TC30GENIChomozygous114940175
6110990115110990116TC44GENIChomozygous114940176
6110990738110990739AT20GENIChomozygous114940177