chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
139022433290224333CT30GENIChomozygous66590277
139022542290225423GA16GENICpossibly homozygous66374531
139022568390225684TA6GENIChomozygous66374533
139022527190225272AG20GENICpossibly homozygous66374527
139022528690225287GA21GENIChomozygous66374529
139022576590225766TC15GENIChomozygous66374535
139022576890225769CT16GENIChomozygous66374537
139022614690226147GA22GENIChomozygous66374539
139022640290226403TC38GENIChomozygous66374541
139022695290226953TG35GENIChomozygous66374543
139022750090227501GA30GENIChomozygous66374545
139022772190227722GA25GENIChomozygous66374547
139022849990228500CT27GENIChomozygous66374549
139022961390229614CA25GENIChomozygous66374551
139023067990230680CT29GENIChomozygous66374553
139023429290234293TG18GENIChomozygous66374555
139023522390235224CT25GENIChomozygous66374557
139023544290235443GT32GENIChomozygous66374559
139023652890236529AT29GENIChomozygous66374561
139023667190236672GA21GENIChomozygous66374563
139023770490237705AG35GENIChomozygous66374565
139023832990238330CA35GENIChomozygous66374567
139023918490239185CT29GENIChomozygous66374569