chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5155916797155916798CT22GENIChomozygous114066163
5155916920155916921AG26GENIChomozygous114066165
5155918900155918901AG6GENIChomozygous114066169
5155919313155919314CT16GENIChomozygous114066171
5155919390155919391TC11GENIChomozygous114066173
5155919426155919427CT12GENIChomozygous114066175
5155919827155919828AT14GENIChomozygous114066177
5155920055155920056TG22GENICpossibly homozygous114066179
5155920089155920090GA20GENIChomozygous114066181
5155920281155920282GA25GENIChomozygous114066187
5155920803155920804CG18GENIChomozygous114066196
5155921056155921057CT21GENIChomozygous114066198
5155921737155921738GA15GENIChomozygous114066200
5155921958155921959CT12GENIChomozygous114066202