chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X124722798124722799TA10GENIChomozygous108811688
X124724768124724769TG3GENIChomozygous108811690
X124724769124724770GT3GENIChomozygous108811692
X124725082124725083AG14GENIChomozygous108326273
X124725898124725899CG14GENIChomozygous108424725
X124726205124726206GA8GENIChomozygous108326275
X124731446124731447TC11GENIChomozygous108811694
X124731973124731974AC7GENIChomozygous108326277
X124732732124732733CT15GENIChomozygous108811696
X124733992124733993TC15GENICpossibly homozygous108811698
X124735405124735406CT14GENIChomozygous108811700
X124735503124735504AG15GENIChomozygous108811702
X124737429124737430GA8GENIChomozygous108811704
X124741491124741492TC15GENIChomozygous108326281
X124742681124742682AG13GENIChomozygous108424727
X124742805124742806CG19GENIChomozygous108811706
X124743157124743158GA14GENIChomozygous108811708
X124743427124743428AC18GENIChomozygous108326283
X124743935124743936AG8GENIChomozygous108326285
X124744260124744261TC20GENICpossibly homozygous108811710
X124744794124744795CT5GENIChomozygous108811712
X124744963124744964CG5GENIChomozygous108811714
X124746581124746582CT12GENIChomozygous108811716
X124747331124747332GA12GENIChomozygous108326293
X124748552124748553TA12GENIChomozygous108326295
X124751603124751604GA11GENIChomozygous108811718
X124755361124755362AG14GENIChomozygous108811720
X124757735124757736AG9GENIChomozygous108326311
X124759073124759074GA12GENIChomozygous108811722