chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185604257956042580AG53GENIChomozygous110542764
185604262456042625TG56GENICpossibly homozygous110542766
185604273256042733GA58GENIChomozygous110542768
185604371656043717AG49GENIChomozygous110542770
185604383356043834TC50GENIChomozygous110542772
185604386356043864TC52GENIChomozygous110542774
185604395956043960GA36GENIChomozygous110542776
185604396556043966CG40GENIChomozygous110542778
185604504756045048AG43GENIChomozygous110592628
185604514056045141AC39GENIChomozygous110542780
185604611256046113GA38GENIChomozygous110542782
185604611956046120GC38GENIChomozygous110542784
185604622756046228AG37GENIChomozygous110542786
185604650656046507GT20GENICheterozygous110542790
185604650956046510GA14GENICheterozygous110813784
185604654656046547GA19GENIChomozygous110542792
185604661356046614CT23GENIChomozygous110592630
185604663756046638CT19GENIChomozygous110875808
185604693956046940CT37GENIChomozygous110542794
185604712156047122AT24GENIChomozygous110542796