chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2257454344257454345AG20GENIChomozygous110411978
2257455127257455128TC21GENIChomozygous111196818
2257457070257457071AT20GENIChomozygous110411982
2257457193257457194GA19GENIChomozygous111196822
2257457204257457205GA23GENIChomozygous110411984
2257459373257459374CT18GENIChomozygous110411988
2257459694257459695CT33GENIChomozygous111196824
2257460164257460165GA22GENIChomozygous111196826
2257461293257461294GC23GENIChomozygous111196828
2257463039257463040TG11GENIChomozygous111196830
2257464195257464196CT19GENICpossibly homozygous111196832
2257464376257464377TC30GENIChomozygous111196834
2257467623257467624CG26GENIChomozygous111196836
2257468979257468980GA21GENIChomozygous111196838
2257469117257469118CT28GENIChomozygous111196840
2257469677257469678AG17GENIChomozygous111196844
2257469983257469984AT12GENIChomozygous111196848
2257470824257470825GA17GENIChomozygous110412000
2257471156257471157GA15GENIChomozygous111196850
2257471175257471176TG16GENIChomozygous110412002
2257473274257473275GA22GENIChomozygous111196852
2257475265257475266AC17GENIChomozygous110412008
2257476720257476721AG19GENIChomozygous111196856
2257477255257477256AG24GENIChomozygous111196858
2257477346257477347GA27GENIChomozygous111196860
2257479169257479170TC25GENIChomozygous111196862
2257480123257480124AG22GENIChomozygous110412010
2257480886257480887AG29GENIChomozygous110412012
2257482144257482145TC27GENIChomozygous111196866
2257482308257482309AG16GENIChomozygous111196868