chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3110671575110671576GA34GENIChomozygous111673163
3110672871110672872CA41GENIChomozygous111673165
3110673349110673350TA35GENIChomozygous111673167
3110674149110674150CG38GENIChomozygous111673168
3110674465110674466TC50GENIChomozygous111673170
3110674854110674855AG54GENIChomozygous111673172
3110676197110676198GT48GENIChomozygous111673173
3110676200110676201TA46GENIChomozygous111673175
3110676206110676207GT42GENICpossibly homozygous111673177
3110678560110678561AG34GENICheterozygous111673179
3110678564110678565AG32GENICheterozygous111673181
3110679217110679218CT46GENIChomozygous111673183
3110682411110682412GA49GENIChomozygous111673185
3110683140110683141TC12GENIChomozygous111673187
3110683391110683392CT48GENIChomozygous111673188
3110684387110684388AC43GENIChomozygous111673190
3110684496110684497CT62GENIChomozygous111673192
3110689389110689390AG42GENIChomozygous111673194