chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1461742416174242GA16GENIChomozygous994924822
1461743086174309CT12GENIChomozygous994924823
1461746646174665AC22GENIChomozygous994924824
1461747076174708AG15GENIChomozygous994924825
1461748706174871TG16GENIChomozygous994924826
1461750996175100GC25GENIChomozygous994924827
1461762496176250TC21GENIChomozygous994924828
1461767686176769AT22GENIChomozygous994924829
1461771496177150TC30GENIChomozygous994924830
1461774006177401GC25GENIChomozygous994924831
1461774566177457TC36GENIChomozygous994924832
1461775596177560AG26GENIChomozygous994924833
1461776266177627AG31GENIChomozygous994924834
1461811396181140GA23GENIChomozygous994924835
1462173686217369CT29GENIChomozygous994924836
1462178456217846CT23GENIChomozygous994924837
1462179876217988CT19GENIChomozygous994924838
1462182606218261AG23GENIChomozygous994924839
1462188826218883CG18GENIChomozygous994924840
1462191226219123CT22GENIChomozygous994924841
1462193136219314CT19GENIChomozygous994924842
1462202146220215CG18GENIChomozygous994924843
1462207146220715AG23GENIChomozygous994924844