chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185604257956042580AG13GENIChomozygous110542764
185604262456042625TG17GENICpossibly homozygous110542766
185604273256042733GA18GENIChomozygous110542768
185604371656043717AG22GENIChomozygous110542770
185604383356043834TC24GENIChomozygous110542772
185604386356043864TC17GENIChomozygous110542774
185604395956043960GA23GENIChomozygous110542776
185604396556043966CG24GENIChomozygous110542778
185604491656044917CA35GENIChomozygous110592626
185604504756045048AG32GENIChomozygous110592628
185604514056045141AC29GENIChomozygous110542780
185604611256046113GA22GENIChomozygous110542782
185604611956046120GC23GENIChomozygous110542784
185604622756046228AG15GENIChomozygous110542786
185604654656046547GA9GENIChomozygous110542792
185604661356046614CT14GENIChomozygous110592630
185604663756046638CT19GENIChomozygous110875808
185604693956046940CT14GENIChomozygous110542794
185604712156047122AT25GENIChomozygous110542796