chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2061234506123451AG27GENIChomozygous63345499
2061235316123532TC30GENIChomozygous63345501
2061239736123974GT17GENIChomozygous63345502
2061240136124014CT16GENIChomozygous63345504
2061241086124109AG20GENIChomozygous63345506
2061243656124366TG29GENIChomozygous63345507
2061245696124570AG35GENIChomozygous63345509
2061252566125257AG38GENIChomozygous63345510
2061255886125589AC38GENIChomozygous63345511
2061259466125947CT41GENIChomozygous63345513
2061265296126530AG28GENIChomozygous63345514
2061267616126762CT33GENIChomozygous63345516
2061273556127356TC23GENIChomozygous63345517
2061273576127358AG22GENIChomozygous63345519
2061276396127640AC21GENIChomozygous63345520
2061276476127648TC21GENIChomozygous63345522
2061277966127797TC21GENIChomozygous63345524
2061278896127890TC21GENIChomozygous63345525
2061283266128327CT13GENIChomozygous63345529
2061283436128344CA13GENIChomozygous63345530
2061283956128396AG15GENIChomozygous63345532
2061283966128397CG15GENIChomozygous63345533
2061284546128455CA10GENIChomozygous84963997
2061284556128456AG10GENIChomozygous64225946
2061284576128458TC10GENIChomozygous64225948
2061284926128493TC16GENIChomozygous63345535
2061286556128656AG17GENIChomozygous63345537
2061287976128798TC9GENIChomozygous63345538