chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
139022527190225272AG19GENICpossibly homozygous66374527
139022528690225287GA18GENIChomozygous66374529
139022542290225423GA19GENIChomozygous66374531
139022568390225684TA14GENIChomozygous66374533
139022576590225766TC15GENIChomozygous66374535
139022576890225769CT15GENIChomozygous66374537
139022614690226147GA26GENIChomozygous66374539
139022640290226403TC28GENIChomozygous66374541
139022695290226953TG24GENIChomozygous66374543
139022750090227501GA15GENIChomozygous66374545
139022772190227722GA17GENIChomozygous66374547
139022849990228500CT39GENIChomozygous66374549
139022961390229614CA26GENIChomozygous66374551
139023067990230680CT28GENIChomozygous66374553
139023429290234293TG34GENIChomozygous66374555
139023522390235224CT12GENIChomozygous66374557
139023544290235443GT18GENIChomozygous66374559
139023652890236529AT27GENIChomozygous66374561
139023667190236672GA28GENIChomozygous66374563
139023770490237705AG40GENIChomozygous66374565
139023832990238330CA38GENIChomozygous66374567
139023918490239185CT16GENIChomozygous66374569
139023474290234743GT44GENIChomozygous66142750