chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
162136512821365129GC20GENIChomozygous111754517
162136568021365681TC18GENIChomozygous111754519
162136815221368153AT20GENIChomozygous111754521
162137040121370402AC24GENIChomozygous111754523
162137048221370483AG9GENIChomozygous111754525
162137076321370764TC16GENIChomozygous112401102
162137100121371002AG22GENIChomozygous111754527
162137104821371049CT26GENIChomozygous111754529
162137127921371280AG22GENIChomozygous111754531
162137132521371326AG18GENIChomozygous111754533
162137238321372384GT25GENIChomozygous111754535
162137389721373898GA26GENIChomozygous111754537
162137433321374334AT10GENIChomozygous111754539
162137434321374344AG7GENIChomozygous111754541
162137461421374615GA23GENIChomozygous111754543
162137509321375094CT12GENIChomozygous111754545
162137532621375327CT23GENIChomozygous111754547
162137612921376130CG17GENICpossibly homozygous111754549
162137695821376959TC22GENIChomozygous111754551
162137831921378320CT17GENIChomozygous111754553
162137869521378696CT14GENICheterozygous111754555
162137869621378697TC14GENIChomozygous111754557
162137897421378975GA24GENIChomozygous111754559
162137946821379469CA5GENIChomozygous125654358