chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106976677869766779TC34GENIChomozygous626123628
106976752069767524TGTC----16GENIChomozygous743074434
106977256869772569GGA33GENIChomozygous743074435
106977403269774033CCT2GENIChomozygous743074437
106977533069775331TG28GENIChomozygous626123629
106977570969775710CT26GENIChomozygous626123630
106977675269776754AA--19GENICpossibly homozygous743074438
106977675369776754A-19GENICheterozygous743074439
106977728169777282CT23GENIChomozygous626123631
106977959669779598CA--26GENICheterozygous743074440
106978177369781774CG20GENIChomozygous626123632
106978200369782004AG17GENIChomozygous626123633
106978244069782441TC22GENIChomozygous626123634
106978668069786681CCT33GENIChomozygous743074441
106978695369786954TC48GENIChomozygous626123635
106978747069787471AG37GENIChomozygous626123636
106978780069787801AG28GENIChomozygous626123637
106978792569787926TC33GENIChomozygous626123638