chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X124722798124722799TA3GENIChomozygous108811688
X124726205124726206GA2GENIChomozygous108326275
X124731446124731447TC2GENIChomozygous108811694
X124731973124731974AC3GENIChomozygous108326277
X124732732124732733CT3GENIChomozygous108811696
X124735405124735406CT4GENIChomozygous108811700
X124737429124737430GA2GENIChomozygous108811704
X124741491124741492TC4GENIChomozygous108326281
X124743157124743158GA4GENIChomozygous108811708
X124743427124743428AC3GENIChomozygous108326283
X124743935124743936AG4GENIChomozygous108326285
X124725898124725899CG2GENIChomozygous108424725
X124742681124742682AG3GENIChomozygous108424727
X124744794124744795CT2GENIChomozygous108811712
X124747331124747332GA4GENIChomozygous108326293
X124751603124751604GA3GENIChomozygous108811718
X124755361124755362AG4GENIChomozygous108811720