chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5139962749139962750AG14GENIChomozygous114029414
5139965305139965306AC10GENIChomozygous114029415
5139966320139966321GC28GENIChomozygous114029416
5139966707139966708CA16GENIChomozygous114029417
5139966958139966959GA13GENIChomozygous114029418
5139964879139964926GCCTTGAAATGCGGGAGTCTGTCATAGCCACCCAGCAACAAGGGCCT6GENIChomozygous128246403
5139970850139970851C2GENIChomozygous129917074
5139971684139971685GA15GENIChomozygous114029424
5139972196139972196GGGTT3GENIChomozygous134285093
5139972648139972665GTGTGTGTGTGTGTGTG4GENIChomozygous129917081
5139972750139972751T7GENIChomozygous129917082
5139972777139972778TA10GENIChomozygous114029425
5139972782139972784TG10GENIChomozygous129917083
5139972810139972810A9GENIChomozygous129917084
5139972841139972841TAC14GENIChomozygous129917085
5139972843139972845AG14GENIChomozygous129917086
5139972854139972854C16GENIChomozygous129917087
5139972873139972874G18GENIChomozygous129917088
5139972925139972925G15GENIChomozygous128246422
5139972939139972940G15GENIChomozygous128246423
5139972998139972998A14GENIChomozygous128246424
5139973007139973007C11GENIChomozygous128246425
5139973018139973019T10GENIChomozygous128246426
5139973037139973038G10GENIChomozygous128246427
5139973041139973041C10GENIChomozygous128246428
5139973061139973062T11GENIChomozygous128246429
5139973065139973066CT11GENIChomozygous114029426
5139973077139973078TC13GENIChomozygous114029427
5139973116139973117CT16GENIChomozygous119084955
5139973145139973146CT10GENIChomozygous114029428
5139973180139973181GC8GENIChomozygous114029429
5139973202139973202AC6GENIChomozygous129917089
5139973234139973234A3GENIChomozygous134285094
5139974975139974976TC18GENIChomozygous114029431
5139975145139975146TC25GENIChomozygous114029432
5139977934139977935AG14GENIChomozygous114029433
5139972201139972202CT3GENIChomozygous134287265
5139972200139972201CA3GENIChomozygous134287264