chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135624347356243474CA35GENICpossibly homozygous142380128
135624496556244966GT33GENIChomozygous139308068
135624508056245081GC34GENIChomozygous143585508
135624516056245161TG40GENIChomozygous139308069
135624570856245709TG51GENIChomozygous139308070
135624586856245869GT35GENIChomozygous139308071
135624611456246115GA61GENIChomozygous139308072
135624703156247032GC42GENIChomozygous139308073
135624884756248848TC41GENIChomozygous139308074
135625044056250441AT49GENIChomozygous139308075
135625135756251358TC48GENIChomozygous144932098
135624844356248444AT53GENIChomozygous144932095
135624885956248860TC47GENIChomozygous144932096
135624890356248904GA47GENIChomozygous144932097
135625065356250655TT7GENIChomozygous144925394
135624753856247538TC15GENIChomozygous139176189
135625084256250842T40GENIChomozygous139176193
135624757956247579CTCTCC11GENICheterozygous145152160
135624762956247630G12GENICheterozygous403339650
135624762956247630GC12GENICpossibly homozygous403339651
135625135856251359GT48GENIChomozygous144932099
135625172056251720A41GENIChomozygous142346222
135625442156254422TC50GENIChomozygous139308078
135625613456256135TA45GENIChomozygous143585509
135625655056256551T28GENIChomozygous139176195
135625716256257163AT42GENIChomozygous143585510
135625720556257206GA43GENIChomozygous139308079
135625802156258022GA57GENIChomozygous143585511
135626035156260352CT45GENIChomozygous139308081
135626073956260740CG41GENIChomozygous139308082
135626134656261347TC56GENIChomozygous139308083
135626202856262029TG42GENIChomozygous154814492
135626202856262029T42GENICheterozygous403339652
135626272656262726T62GENIChomozygous139176197
135626543456265435GA42GENIChomozygous139308084
135626558356265584T43GENICpossibly homozygous139176198
135626584656265847TC43GENIChomozygous143585513