chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
15106800722106800723CT41GENIChomozygous112640249
15106800872106800873TC71GENIChomozygous112640251
15106801670106801671AT12GENIChomozygous112640253
15106802516106802517AG37GENIChomozygous112640255
15106803588106803589AG43GENIChomozygous112640259
15106804191106804192AG43GENIChomozygous112640261
15106805214106805215GA53GENIChomozygous112640263
15106805677106805678GA27GENIChomozygous112640265
15106805821106805822TC49GENIChomozygous112640267
15106803886106803887GA7GENIChomozygous112767757
15106806941106806942CA38GENIChomozygous112640269
15106812513106812514AT26GENIChomozygous112640273
15106812741106812742GA23GENIChomozygous112640275
15106814416106814417CT20GENIChomozygous112640277
15106817380106817381GA37GENIChomozygous112640279
15106818407106818408GA41GENIChomozygous112640281
15106823434106823435TC47GENIChomozygous112640283
15106827341106827342GA52GENIChomozygous112640285
15106827342106827343AG53GENIChomozygous112640287
15106829918106829919CA50GENIChomozygous112640289
15106834050106834051AG35GENIChomozygous112640291
15106834240106834241AG50GENIChomozygous112640293
15106836229106836230TC35GENIChomozygous112640295
15106836272106836273GA31GENIChomozygous112640297
15106837047106837048AG24GENIChomozygous112640299
15106837901106837902TA9GENIChomozygous112640301
15106842048106842049AC24GENIChomozygous112640303
15106842555106842556TC26GENIChomozygous112640305
15106843104106843105TC15GENIChomozygous112640307