chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18156012381560124TC11GENIChomozygous61882531
18156022381560224CG10GENIChomozygous61882532
18156061981560621GC--22GENIChomozygous60746734
18156062281560623CCAAAAACATTT22GENIChomozygous62136340
18156133281561333AG13GENICpossibly homozygous62136341
18156192481561926AA--8GENICpossibly homozygous62136342
18156234381562344A-10GENIChomozygous62136343
18156353181563532AG37GENIChomozygous62136344
18156415781564158TG22GENIChomozygous62136345
18156419381564194GA22GENIChomozygous62136346
18156519381565194TC20GENICpossibly homozygous62136347
18156663881566639TC10GENIChomozygous62136348
18156674481566745GC14GENIChomozygous62136349
18156688381566884GA18GENIChomozygous62136350
18156698381566985TC--19GENIChomozygous62136351
18156710681567107CG18GENIChomozygous62136352
18156735081567351AC29GENIChomozygous62136353
18156751581567516AC27GENICpossibly homozygous62136354
18156858381568584CT27GENIChomozygous62136355
18157031181570312TC29GENICpossibly homozygous61882537
18157227381572274TA27GENIChomozygous62136356
18157242881572429GT24GENIChomozygous62136357
18157252381572524TA18GENIChomozygous62083737
18157273481572735AG25GENIChomozygous62136358