chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1157172470157172471AG13GENICheterozygous74563325
1157175308157175309GA41GENIChomozygous74563328
1157175741157175742AG23GENICheterozygous74563331
1157175883157175884AG22GENIChomozygous74563334
1157176060157176061GA36GENIChomozygous74563337
1157176188157176189GT31GENIChomozygous74563340
1157176430157176431GA35GENIChomozygous74563343
1157179762157179763TC23GENICpossibly homozygous76689600
1157177977157177978GA28GENIChomozygous76689596
1157178915157178916GC23GENIChomozygous76689597
1157179121157179122CT35GENIChomozygous76689598
1157179331157179332CT42GENIChomozygous76689599
1157180040157180041AG27GENICpossibly homozygous75150213
1157180200157180201TC33GENIChomozygous75150214