chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5139962749139962750AG15GENIChomozygous114029414
5139965305139965306AC10GENIChomozygous114029415
5139966320139966321GC23GENIChomozygous114029416
5139966707139966708CA25GENIChomozygous114029417
5139966958139966959GA16GENIChomozygous114029418
5139964879139964926GCCTTGAAATGCGGGAGTCTGTCATAGCCACCCAGCAACAAGGGCCT3GENIChomozygous128246403
5139971684139971685GA15GENIChomozygous114029424
5139972240139972240GCAAGC9GENIChomozygous128246421
5139973007139973007C19GENIChomozygous128246425
5139972925139972925G14GENIChomozygous128246422
5139972939139972940G17GENIChomozygous128246423
5139972998139972998A20GENIChomozygous128246424
5139973018139973019T16GENIChomozygous128246426
5139973037139973038G16GENIChomozygous128246427
5139973041139973041C16GENIChomozygous128246428
5139973061139973062T14GENIChomozygous128246429
5139973065139973066CT13GENIChomozygous114029426
5139973077139973078TC13GENIChomozygous114029427
5139973145139973146CT9GENIChomozygous114029428
5139973180139973181GC4GENIChomozygous114029429
5139973202139973202AC4GENIChomozygous129917089
5139974975139974976TC17GENIChomozygous114029431
5139975145139975146TC15GENIChomozygous114029432
5139977934139977935AG21GENIChomozygous114029433
5139973116139973117CT12GENIChomozygous119084955