chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1261483931261483932TC20GENIChomozygous125494295
1261484477261484478AT15GENIChomozygous125382991
1261485251261485252GA14GENIChomozygous125494296
1261485579261485580GA8GENIChomozygous125471559
1261485675261485676CT14GENIChomozygous125382992
1261486334261486335AG14GENIChomozygous125382993
1261486471261486472AG15GENIChomozygous125382994
1261486941261486942AG12GENIChomozygous125382995
1261486962261486963AG11GENIChomozygous125471560
1261486963261486964TC11GENIChomozygous125471561
1261487631261487632GT4GENIChomozygous125382996
1261488441261488442CT6GENIChomozygous125382998
1261488824261488825TC25GENIChomozygous125382999
1261488872261488873CT13GENIChomozygous125471562
1261489176261489177AG12GENIChomozygous125383000
1261489226261489227CT11GENIChomozygous125383001
1261489364261489365AG12GENIChomozygous125383003
1261489530261489531AT7GENIChomozygous125383004
1261489594261489595GA16GENIChomozygous125383005
1261490087261490088CT10GENIChomozygous125383006
1261490111261490112GA8GENIChomozygous125471563
1261490216261490217GA8GENIChomozygous125383007
1261490305261490306AG15GENIChomozygous125383008
1261490621261490622GC13GENIChomozygous125383009
1261490712261490713AG17GENIChomozygous125383010
1261490927261490928TC19GENIChomozygous125383011
1261491032261491033AG14GENIChomozygous125383012
1261491242261491243AG4GENIChomozygous125383013
1261491377261491378AG14GENIChomozygous125383014
1261491461261491462AG15GENIChomozygous125383015
1261491675261491676GC15GENIChomozygous125383016
1261492261261492262CT12GENIChomozygous125383017
1261492295261492296TC20GENIChomozygous125383018
1261492629261492630TC12GENIChomozygous125383019
1261493547261493548AT14GENIChomozygous125383021
1261494158261494159GC11GENIChomozygous125383022
1261494315261494316CT5GENIChomozygous125383023
1261494321261494322TG4GENIChomozygous125383024