chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3175701358175701359AG51GENIChomozygous112218188
3175702108175702109GA49GENIChomozygous112218189
3175702617175702618TC37GENIChomozygous112218190
3175703187175703188AG47GENICpossibly homozygous112218192
3175703534175703535AG42GENIChomozygous112218194
3175703845175703846AG45GENIChomozygous112218195
3175703941175703942TC39GENIChomozygous112218196
3175705369175705370CT41GENIChomozygous112218197
3175706974175706975AG46GENIChomozygous112218198
3175709397175709398AG41GENIChomozygous112218199