chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2208530003208530004GC18GENICheterozygous59932302
2208530309208530310G-31GENIChomozygous59358153
2208532431208532432AG26GENIChomozygous59358154
2208533055208533056CT28GENICpossibly homozygous60159102
2208533056208533057AG28GENICpossibly homozygous60159103
2208533934208533935TG50GENIChomozygous59358155
2208534119208534128AGGGTCCTG---------11GENIChomozygous59932304
2208535576208535582CTGCCT------11GENIChomozygous59358156
2208536076208536077AG29GENIChomozygous59358159
2208536100208536101TC34GENIChomozygous59358160
2208536109208536110GA33GENIChomozygous60159104
2208537846208537847GGT46GENIChomozygous59932307