chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
139022527190225272AG7GENICpossibly homozygous66374527
139022528690225287GA11GENIChomozygous66374529
139022542290225423GA4GENICheterozygous66374531
139022568390225684TA8GENIChomozygous66374533
139022576590225766TC11GENIChomozygous66374535
139022576890225769CT13GENIChomozygous66374537
139022614690226147GA19GENIChomozygous66374539
139022640290226403TC14GENIChomozygous66374541
139022695290226953TG16GENIChomozygous66374543
139022750090227501GA15GENIChomozygous66374545
139022772190227722GA13GENIChomozygous66374547
139022849990228500CT9GENIChomozygous66374549
139022961390229614CA6GENIChomozygous66374551
139023067990230680CT10GENIChomozygous66374553
139023429290234293TG3GENIChomozygous66374555
139023522390235224CT7GENIChomozygous66374557
139023544290235443GT10GENIChomozygous66374559
139023652890236529AT7GENIChomozygous66374561
139023667190236672GA4GENIChomozygous66374563
139023770490237705AG9GENIChomozygous66374565
139023918490239185CT7GENIChomozygous66374569
139023997290239973GA7GENICheterozygous67643219