chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8115761506115761507CT18GENIChomozygous52826692
8115762581115762582TC14GENIChomozygous52826694
8115762799115762800TTAC12GENIChomozygous52826695
8115762927115762928CT11GENIChomozygous53167828
8115765168115765169T-6GENIChomozygous53050710
8115765540115765541GT31GENIChomozygous53167830
8115765572115765573GA36GENIChomozygous52826698
8115766556115766557A-4GENIChomozygous52826699
8115766589115766591AA--5GENIChomozygous52826700
8115766980115766981CT8GENIChomozygous52826701
8115767357115767358TC15GENIChomozygous52826703
8115767612115767613TC25GENIChomozygous52826704
8115768827115768830TCT---18GENIChomozygous52826705
8115769039115769040TG27GENIChomozygous52826706
8115769090115769091GGCTGGAAGGTC33GENIChomozygous52826707
8115769867115769868TC17GENIChomozygous52826708
8115774865115774868AAC---20GENIChomozygous53167832
8115775284115775285CT22GENIChomozygous52826715
8115775712115775713GGCACACACACACACA23GENIChomozygous53411154
8115775872115775873GA25GENIChomozygous52826718
8115776604115776605AG25GENIChomozygous52826723
8115778236115778237CA27GENIChomozygous52826726
8115778902115778903AG23GENIChomozygous52826727