chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X116088837116088838GT18GENIChomozygous140688009
X116089419116089420T24GENIChomozygous140593761
X116090391116090392GA22GENIChomozygous140688010
X116091707116091708GA22GENIChomozygous140688011
X116092156116092157CA23GENIChomozygous140688012
X116092581116092581T25GENIChomozygous140593762
X116093595116093596GC21GENIChomozygous140688013
X116096050116096051TC20GENIChomozygous140688014
X116096149116096149A5GENIChomozygous140593765
X116099364116099365GT21GENIChomozygous140688015
X116096270116096270A5GENIChomozygous142746282
X116103463116103464A18GENIChomozygous140593766
X116106050116106051TC20GENIChomozygous140688016
X116108364116108364T21GENIChomozygous140593767
X116112914116112915TC22GENIChomozygous140688017
X116113134116113135CT21GENIChomozygous140688018