chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
98015457180154572AG50GENIChomozygous120270028
98015464380154644GA51GENIChomozygous120270029
98015469680154697AC54GENIChomozygous120270030
98015496980154970TC57GENIChomozygous120270031
98015499180154992GT52GENIChomozygous120270032
98015517780155178CT74GENIChomozygous120270033
98015553180155532GA64GENIChomozygous120270034
98015566480155665AG53GENIChomozygous120270035
98015598380155984GA58GENIChomozygous120270036
98015602280156023AG65GENIChomozygous120270037
98015620180156202AT50GENIChomozygous120270038
98015631080156311TC59GENIChomozygous120270039
98015639880156399CA55GENIChomozygous120270040
98015645280156453GA51GENIChomozygous120270041
98015686580156866A42GENICpossibly homozygous128727205
98015752680157527AG55GENIChomozygous120270042
98015766680157667AG45GENIChomozygous120270043
98015774880157748C45GENICpossibly homozygous131071635
98016015180160152GA55GENIChomozygous117848246
98016042680160427TG54GENICpossibly homozygous117848247
98016155180161552A46GENIChomozygous131071636
98016251980162520A52GENIChomozygous128727206
98016303080163031GA51GENIChomozygous117848248
98016340280163403TC52GENIChomozygous117879389
98016381180163812AT52GENIChomozygous117879393
98016654580166546GC50GENIChomozygous117848251
98016654880166549GT51GENIChomozygous117879399