chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135624347356243474CA35GENICpossibly homozygous142380128
135624496556244966GT28GENIChomozygous139308068
135624508056245081GC41GENIChomozygous143585508
135624516056245161TG44GENIChomozygous139308069
135624570856245709TG69GENIChomozygous139308070
135624586856245869GT34GENICpossibly homozygous139308071
135624611456246115GA43GENIChomozygous139308072
135624703156247032GC48GENIChomozygous139308073
135624884756248848TC56GENIChomozygous139308074
135625044056250441AT52GENIChomozygous139308075
135624753856247538TC15GENIChomozygous139176189
135624844356248444AT57GENIChomozygous144932095
135624885956248860TC57GENIChomozygous144932096
135624890356248904GA53GENIChomozygous144932097
135625084256250842T49GENIChomozygous139176193
135625135756251358TC50GENIChomozygous144932098
135625135856251359GT49GENIChomozygous144932099
135625172056251720A64GENICpossibly homozygous142346222
135625442156254422TC49GENIChomozygous139308078
135625613456256135TA45GENIChomozygous143585509
135625655056256551T42GENIChomozygous139176195
135625716256257163AT46GENIChomozygous143585510
135625720556257206GA51GENIChomozygous139308079
135625802156258022GA53GENIChomozygous143585511
135626035156260352CT59GENIChomozygous139308081
135626073956260740CG58GENIChomozygous139308082
135626134656261347TC78GENIChomozygous139308083
135626272656262726T50GENIChomozygous139176197
135626543456265435GA50GENIChomozygous139308084
135626584656265847TC43GENIChomozygous143585513
135625065356250655TT17GENICpossibly homozygous144925394
135626558356265584T56GENIChomozygous139176198