chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
56179891861798919CG18GENIChomozygous827079993
56180017461800175GGC9GENIChomozygous827079994
56180020061800201A-11GENIChomozygous827079995
56180027661800277TTATA16GENIChomozygous827079996
56180033961800340AG18GENIChomozygous827079997
56180082961800830GA16GENIChomozygous827079998
56180095361800954TTTTTA10GENIChomozygous827079999
56180122561801226AG17GENIChomozygous827080000
56180192061801921AT13GENIChomozygous827080001
56180226261802263TC18GENIChomozygous827080002
56180234161802342TA16GENIChomozygous827080003
56180268661802691TTGTT-----10GENIChomozygous827080004
56180274561802746TC15GENIChomozygous827080005
56180289561802896TG22GENIChomozygous827080006
56180308061803081CT13GENIChomozygous827080007
56180361461803615GA12GENIChomozygous827080008
56180363961803640CT12GENIChomozygous827080009
56180374461803745GA7GENIChomozygous827080010
56180424561804246GA13GENIChomozygous827080011
56180566561805666AG17GENIChomozygous827080012
56180567061805671AG17GENIChomozygous827080013
56180629261806293CT8GENIChomozygous827080014
56180761461807615TC16GENIChomozygous827080015
56180891761808918GA13GENIChomozygous827080016
56180949961809500TC15GENIChomozygous827080017
56180985561809861GAGGCA------8GENIChomozygous827080018
56181175561811756CT11GENIChomozygous827080019
56181238961812390TC10GENIChomozygous827080020
56181263261812633GT13GENIChomozygous827080021
56181339661813397CT8GENIChomozygous827080022
56181381161813812AG11GENIChomozygous827080023
56181406261814066AAAA----7GENIChomozygous827080024
56181455861814559GA10GENIChomozygous827080025
56181516761815168AG11GENIChomozygous827080026