chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
204078266740782668TA50GENIChomozygous109267071
204078279640782797TC69GENICheterozygous119820926
204078280040782801TC68GENICheterozygous119820927
204078389040783891TA89GENICheterozygous119820928
204078389640783897CT86GENICheterozygous119820929
204078391340783914AG81GENICheterozygous119820930
204078484240784843TC59GENIChomozygous109267075
204078546140785462GA72GENIChomozygous109315162
204078400740784008AG69GENIChomozygous109315158
204078512740785128GA27GENIChomozygous109315160
204078576340785764CT73GENIChomozygous109315164
204078585740785858TG68GENIChomozygous109315166
204078589840785899TG74GENIChomozygous109315168
204078616840786169TC43GENIChomozygous109465284
204078621540786216AG44GENIChomozygous119820931
204078875040788751CA80GENICheterozygous119820932
204078913240789133AT87GENICheterozygous119820933
204079021240790213GA29GENIChomozygous119820934
204079039940790400AT39GENIChomozygous119820935
204079046640790467CT41GENIChomozygous119820936
204079052540790526CT44GENIChomozygous119820937
204079055040790551AG47GENIChomozygous119820938
204079057540790576CA55GENICpossibly homozygous109315170
204079313140793132GT70GENIChomozygous109315172
204079344140793442AG85GENICpossibly homozygous109267083
204079355840793559AG65GENIChomozygous109267085
204079467040794671GT81GENIChomozygous109315174
204078681240786813CT38GENIChomozygous109401529
204079549440795495AT50GENICpossibly homozygous109315176
204079607340796074GC57GENIChomozygous109315178
204079632340796324AG49GENICpossibly homozygous109267097
204079694840796949AG53GENIChomozygous109267099
204079728640797287AG85GENIChomozygous109267103
204079759240797593CT51GENIChomozygous109315180
204079836940798370AG71GENIChomozygous109267107
204080059740800598TC62GENICpossibly homozygous109267114
204080070440800705GA61GENICpossibly homozygous109267116
204080081540800816TA64GENICpossibly homozygous109267122