chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5138421203138421204AG39GENIChomozygous55902572
5138422055138422056CT48GENICpossibly homozygous55747424
5138422218138422219AG44GENIChomozygous55747425
5138422308138422309GA41GENIChomozygous55747426
5138422481138422482CT57GENIChomozygous55747427
5138422726138422727CT45GENIChomozygous55747429
5138423285138423286CT47GENIChomozygous55747431
5138423386138423387TC55GENIChomozygous55747432
5138423433138423434GA63GENIChomozygous55902574
5138423481138423482TC75GENICpossibly homozygous55902576
5138423522138423523TA67GENIChomozygous55747433
5138423540138423541CT75GENIChomozygous55902578
5138423586138423587CT64GENIChomozygous55902580
5138424104138424105CT46GENIChomozygous55902582
5138424169138424170AG61GENIChomozygous55902584
5138424177138424178TC59GENIChomozygous55902586
5138424330138424331TA59GENIChomozygous55902588
5138424338138424339TC55GENIChomozygous55902590
5138424777138424778TC56GENIChomozygous55747439
5138424942138424943AG56GENIChomozygous55747440