chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
147709184177091841TTTTATAT39GENIChomozygous129175762
147709186277091862A30GENIChomozygous129175763
147709192977091929C9GENIChomozygous129175764
147709213177092131T34GENIChomozygous129175765
147709669277096694GT37GENICheterozygous131512735
147711844977118449TTTCTTTTA44GENIChomozygous129175776
147711851277118513AC43GENIChomozygous113823909
147711851377118514CA43GENIChomozygous114163762
147717088577170885C52GENIChomozygous129175812
147717092477170924A44GENIChomozygous129175813
147717096977170969C51GENIChomozygous129175815
147717106077171060C48GENIChomozygous129175817
147717281277172813AC62GENIChomozygous113495661
147716051377160513TC4GENICheterozygous130428277
147717106577171066A51GENIChomozygous129175818
147717106877171068T53GENIChomozygous129175819
147717119377171195CC51GENIChomozygous129175820
147717122777171227T51GENIChomozygous129175821
147717285477172854C54GENIChomozygous129175822
147717285877172859G52GENIChomozygous129175823
147717286177172861A53GENIChomozygous129175824
147717315377173154C55GENIChomozygous129175825
147717317877173179C64GENIChomozygous129175826
147717320477173206CA61GENIChomozygous129175827
147717322277173222A59GENIChomozygous129175828
147717323577173236G58GENIChomozygous129175829
147717327277173273C51GENIChomozygous129175830
147717332377173327ACAC39GENIChomozygous129175831
147717292977172930CA57GENIChomozygous113602551
147717913677179136AC34GENIChomozygous129175832
147718765477187654GGGG15GENIChomozygous129175837