chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
51790871217908713GC24GENIChomozygous118851211
51790886517908866GT17GENIChomozygous118851212
51790924017909241GA24GENIChomozygous118851213
51790936717909368GT24GENIChomozygous118851214
51790976917909770CG12GENIChomozygous118851215
51790992717909928GT21GENIChomozygous118851216
51791015117910152TC23GENIChomozygous114476804
51791024317910244TC13GENIChomozygous118851217
51791045017910451GT29GENIChomozygous114476806
51791050817910509TC36GENIChomozygous118851218
51791207417912075TG20GENIChomozygous118851219
51791219017912191CT15GENIChomozygous118851220
51791269817912699TA21GENIChomozygous118851221
51791356917913570TC27GENIChomozygous119027368
51791358917913590CT23GENIChomozygous118851222
51791362317913624AC22GENIChomozygous118851223
51791362717913628AC22GENIChomozygous118851224
51791373417913735GA18GENIChomozygous118851225
51791477917914780AC19GENIChomozygous118851226
51791511417915115GA24GENIChomozygous118851227
51791537917915380AG20GENIChomozygous114476812
51791572317915724GC17GENIChomozygous118851228
51791639217916393GT13GENIChomozygous118851229
51791678917916790CG28GENIChomozygous118851230
51791718417917185TC28GENIChomozygous118851231
51791724117917242TC28GENIChomozygous114476817
51791764017917641CT33GENIChomozygous118851232
51791768317917684GA34GENIChomozygous118851233
51791856417918565CA36GENIChomozygous118851234
51791862917918630CT31GENIChomozygous118851235
51791915017919151TC17GENIChomozygous114476819
51791939417919395AT28GENIChomozygous114476821