chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106777607567776076G10GENICheterozygous128827554
106777610467776105A17GENIChomozygous128827555
106777614667776147C29GENIChomozygous128827556
106777614767776148AT29GENIChomozygous116621206
106777616767776169TG29GENIChomozygous128827557
106777620267776203GC28GENIChomozygous116621208
106777620367776204TG28GENIChomozygous116621210
106777620667776207T28GENIChomozygous128827558
106777621467776215TA27GENIChomozygous116621212
106777621967776220G27GENIChomozygous128827559
106777622667776227TG27GENIChomozygous116621214
106777622767776228GT27GENIChomozygous116621216
106777624167776241G23GENIChomozygous128827560
106777627667776277T57GENIChomozygous128827561
106777630367776304G55GENIChomozygous128827562
106777630767776308A54GENIChomozygous128827563
106777631167776312T54GENIChomozygous128827564
106777632367776323A53GENIChomozygous128827565
106777632967776330G54GENIChomozygous128827566
106777634067776341T49GENIChomozygous128827567
106777635167776352C49GENIChomozygous128827568
106777638467776385G58GENIChomozygous128827569
106777638867776388G58GENIChomozygous128827570
106777639067776391TC55GENIChomozygous116796441
106777640367776404T55GENIChomozygous128827571
106777641967776420A56GENIChomozygous128827572
106777643467776435GA54GENIChomozygous116796443
106777644267776443G57GENIChomozygous128827573