chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108613905586139056TC6GENIChomozygous52572197
108613911486139115TG6GENIChomozygous52572200
108613923286139233CG11GENIChomozygous52572203
108613930486139305GGAATA11GENIChomozygous52572206
108613931486139315CT12GENIChomozygous52572209
108614076486140765C-1GENIChomozygous51527477
108614077386140774CA1GENIChomozygous52163314
108614078286140783C-1GENIChomozygous51527478
108614090686140907CA2GENIChomozygous52572212
108614147686141477AG9GENIChomozygous52572215
108614159686141597GGC7GENICpossibly homozygous52572218
108614180186141802CT5GENIChomozygous52572221
108614240586142406CT6GENIChomozygous52572223
108614308586143086CT6GENIChomozygous52572226
108614315186143152A-9GENIChomozygous52572229
108614343386143434GA5GENIChomozygous52572231
108614397586143976CT8GENIChomozygous52572234
108614421886144219GA7GENIChomozygous52572237
108614453186144532AG10GENIChomozygous52572240
108614495286144953AG5GENIChomozygous52572244
108614571186145712CA7GENIChomozygous52572247
108614582886145829AG17GENIChomozygous52572250
108614618786146188AC9GENIChomozygous52572253
108614653686146537TC5GENIChomozygous52572256
108614744386147444TC11GENIChomozygous52572258
108614757386147574TC4GENIChomozygous52572261
108614795986147960CT7GENIChomozygous52572264
108614810186148102GA9GENIChomozygous52572267
108614852586148526GA6GENIChomozygous52572270
108614860486148736GAAAGCAAGAGATTCTTTTTTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTTTTTTTTTCCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAACC------------------------------------------------------------------------------------------------------------------------------------6GENIChomozygous52322528
108614882586148826TC5GENIChomozygous52572273
108614971286149713TC13GENIChomozygous52572275
108614977086149771AG9GENIChomozygous52572278
108614988186149882GA3GENIChomozygous52572281
108615013486150135GGCTGTGACAC13GENIChomozygous52572284