chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
96165636461656365TA9GENIChomozygous947566309
96165719261657193AC20GENIChomozygous947566310
96165752361657524GA22GENIChomozygous947566311
96165763461657635GT20GENIChomozygous947566312
96165770661657707AG12GENIChomozygous947566313
96165808461658085TC29GENIChomozygous947566314
96165825361658254TA27GENIChomozygous947566315
96165866361658664CT32GENIChomozygous947566316
96165934361659344CT17GENIChomozygous947566317
96165937861659379GA18GENIChomozygous947566318
96166026961660270GC22GENIChomozygous947566319
96166030661660307CT26GENIChomozygous947566320
96166030961660310AC25GENIChomozygous947566321
96166205761662058TC18GENIChomozygous947566322
96166245961662460GT21GENIChomozygous947566323
96166317561663176TA14GENIChomozygous947566324
96166372461663725CT21GENIChomozygous947566325
96166403061664031CG25GENIChomozygous947566326
96166420861664209AG31GENIChomozygous947566327
96166450461664505AG17GENIChomozygous947566328
96166549661665497CA15GENIChomozygous947566329
96166623861666239CT28GENIChomozygous947566330
96166770061667701AG31GENIChomozygous947566331
96166793661667937GA4GENIChomozygous947566332
96167243961672440CT17GENIChomozygous947566333
96167248561672486AG24GENIChomozygous947566334
96167254061672541CT18GENIChomozygous947566335
96167279361672794GA21GENICpossibly homozygous947566336
96167308661673087GC18GENIChomozygous947566337
96167371461673715GA10GENIChomozygous947566338
96167396661673967TC28GENIChomozygous947566339
96167438861674389GT25GENIChomozygous947566340
96167473161674732CT30GENIChomozygous947566341
96167481661674817AT25GENIChomozygous947566342
96167511361675114CT25GENIChomozygous947566343
96167532561675326CT34GENIChomozygous947566344
96167582361675824AC33GENIChomozygous947566345
96167582461675825GA34GENIChomozygous947566346