chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2061234506123451AG49GENIChomozygous63345499
2061235316123532TC53GENIChomozygous63345501
2061239736123974GT44GENIChomozygous63345502
2061240136124014CT34GENIChomozygous63345504
2061241086124109AG39GENIChomozygous63345506
2061243656124366TG53GENIChomozygous63345507
2061245696124570AG44GENIChomozygous63345509
2061252566125257AG75GENIChomozygous63345510
2061255886125589AC63GENIChomozygous63345511
2061259466125947CT81GENIChomozygous63345513
2061265296126530AG37GENIChomozygous63345514
2061267616126762CT42GENIChomozygous63345516
2061273556127356TC56GENICpossibly homozygous63345517
2061273576127358AG57GENIChomozygous63345519
2061276396127640AC44GENIChomozygous63345520
2061276476127648TC44GENIChomozygous63345522
2061277966127797TC40GENIChomozygous63345524
2061278896127890TC20GENIChomozygous63345525
2061280436128044AG26GENIChomozygous63345527
2061283266128327CT61GENIChomozygous63345529
2061283436128344CA54GENICpossibly homozygous63345530
2061283956128396AG33GENIChomozygous63345532
2061283966128397CG33GENIChomozygous63345533
2061284926128493TC33GENIChomozygous63345535
2061286556128656AG48GENIChomozygous63345537
2061287976128798TC14GENIChomozygous63345538
2061288116128812CG9GENICpossibly homozygous63345540