chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
88564184385641844CT38GENICheterozygous116545140
88564192985641930TC42GENIChomozygous116545142
88564214085642141CT45GENICpossibly homozygous116545144
88564238385642384GA51GENICpossibly homozygous116545146
88564264285642643GT51GENICheterozygous116545148
88564264985642650TA50GENICheterozygous116545150
88564272785642728CT53GENICheterozygous116545152
88564275685642757GC47GENICheterozygous116545154
88564278385642784AG33GENICheterozygous116545156
88564278685642787CT32GENICheterozygous116545158
88564434185644342AG13GENIChomozygous116545160
88564447485644475TC37GENIChomozygous116545162
88564459585644596TC10GENIChomozygous116545164
88564505685645057CT60GENICpossibly homozygous116545166
88564506185645062GA58GENICpossibly homozygous116545168
88564507085645071TC50GENIChomozygous116545170
88564519185645192GA71GENICheterozygous116545172
88564534985645350TC58GENIChomozygous116545174
88564560185645602CT49GENIChomozygous116545176