chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1124829459124829460CT15GENIChomozygous108214312
1124829729124829730CG17GENICpossibly homozygous108214313
1124830325124830326TA22GENIChomozygous108214314
1124830518124830519GC10GENIChomozygous108214315
1124830816124830817GA13GENIChomozygous108214316
1124830867124830868CT23GENIChomozygous108214317
1124830922124830923TG11GENIChomozygous108214318
1124830971124830972GA13GENIChomozygous108214319
1124831291124831292CT33GENIChomozygous108214320
1124831563124831564TC17GENIChomozygous108214321
1124831697124831698TG10GENIChomozygous108214322
1124832228124832229TA33GENIChomozygous108214324
1124832925124832926GA23GENIChomozygous108214325
1124832875124832876GT4GENIChomozygous108924447
1124833468124833469CT19GENIChomozygous108214326
1124835536124835537CT13GENIChomozygous108214327