chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
167085569970855700GT22GENIChomozygous112075990
167085590170855902GA16GENIChomozygous112176987
167085992570859926AT15GENIChomozygous112076010
167086000570860006TA18GENIChomozygous112176989
167086032970860330AG17GENIChomozygous112076014
167086054470860545CG31GENIChomozygous112176991
167086162070861621AG10GENIChomozygous119233447
167086212870862129TG15GENIChomozygous112076020
167086217570862176AG13GENIChomozygous112076022
167086264070862641TC14GENIChomozygous112076024
167086383870863839AG13GENIChomozygous112176993
167086413570864136TC9GENIChomozygous112076028
167086476770864768AG12GENIChomozygous112176995
167086518570865186AT22GENIChomozygous112176997
167086533370865334GA5GENICheterozygous112176999
167086557070865571GA13GENIChomozygous112177001
167086600670866007CT22GENIChomozygous112177003
167086626070866261GA26GENIChomozygous112177005
167086649870866499CT12GENIChomozygous112177007
167086678370866784CG23GENIChomozygous112177009
167086737770867378AG20GENIChomozygous112177011
167086742270867423GA7GENIChomozygous112233689
167086743470867435GA14GENIChomozygous112177013
167086795070867951CT15GENIChomozygous112177015
167086806670868067GA22GENIChomozygous112177017
167086810170868102TC16GENIChomozygous112076032
167086812970868130TC9GENIChomozygous112076036
167086832670868327CT15GENIChomozygous112177019
167086840270868403GA37GENIChomozygous112177021
167086850070868501CG15GENIChomozygous112177023
167086954670869547CT20GENIChomozygous112177025
167085945770859458AC8GENIChomozygous112132322
167086256670862567AG6GENIChomozygous119172442