chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
176997525469975255AG57GENIChomozygous111084874
176997583969975840CT44GENIChomozygous111263429
176997593369975933GCAGGCAACACAGCATACAGGCACACTA35GENIChomozygous132217622
176997596869975969TC45GENIChomozygous111263431
176997635069976351AC29GENIChomozygous132223598
176997645169976452GA40GENIChomozygous111263433
176997736469977365TC42GENIChomozygous111084881
176997783369977834CT47GENIChomozygous111212222
176997816769978168TG46GENIChomozygous111263435
176997826069978261GA45GENIChomozygous132223599
176997885569978856GA31GENIChomozygous111358760
176997932469979325CT49GENIChomozygous132223600
176997936669979367AT43GENIChomozygous119299772
176997966469979665CA54GENIChomozygous132223601
176997978769979788TA36GENIChomozygous125560154
176998072469980725AG40GENIChomozygous132223602
176998112669981127TC35GENIChomozygous132223603
176998133369981334AC41GENIChomozygous111559840
176998183569981836TA34GENICpossibly homozygous111084883
176998231769982318GT48GENIChomozygous111084885