chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
167085569970855700GT58GENIChomozygous112075990
167085590170855902GA44GENICheterozygous112176987
167085841370858414TC50GENIChomozygous112076002
167085934370859344TC22GENIChomozygous112076008
167085945770859458AC25GENIChomozygous112132322
167085992570859926AT35GENIChomozygous112076010
167086000570860006TA55GENIChomozygous112176989
167086032970860330AG41GENIChomozygous112076014
167086054470860545CG45GENIChomozygous112176991
167086212870862129TG67GENIChomozygous112076020
167086217570862176AG57GENIChomozygous112076022
167086264070862641TC34GENIChomozygous112076024
167086383870863839AG44GENIChomozygous112176993
167086413570864136TC46GENIChomozygous112076028
167086476770864768AG32GENIChomozygous112176995
167086518570865186AT57GENIChomozygous112176997
167086533370865334GA45GENIChomozygous112176999
167086557070865571GA58GENIChomozygous112177001
167086600670866007CT44GENIChomozygous112177003
167086626070866261GA68GENIChomozygous112177005
167086649870866499CT42GENIChomozygous112177007
167086678370866784CG41GENICpossibly homozygous112177009
167086737770867378AG56GENIChomozygous112177011
167086743470867435GA58GENICpossibly homozygous112177013
167086795070867951CT57GENIChomozygous112177015
167086806670868067GA59GENIChomozygous112177017
167086810170868102TC45GENIChomozygous112076032
167086812970868130TC49GENIChomozygous112076036
167086832670868327CT62GENIChomozygous112177019
167086840270868403GA64GENIChomozygous112177021
167086850070868501CG66GENIChomozygous112177023
167086954670869547CT59GENIChomozygous112177025
167086255170862552TA31GENIChomozygous112233685
167086323970863240CA18GENIChomozygous112233687
167086742270867423GA53GENICpossibly homozygous112233689
167086162070861621AG43GENICpossibly homozygous119233447