chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157865066157865067CT23GENICpossibly homozygous112907536
4157866275157866276C34GENIChomozygous128096370
4157866774157866775C24GENIChomozygous128096371
4157867154157867155CG25GENIChomozygous112907538
4157867573157867574GA16GENIChomozygous112907540
4157867624157867625C12GENIChomozygous128096372
4157868267157868268GA35GENIChomozygous112907542
4157875779157875780AG21GENIChomozygous112907544
4157876195157876195TCTTTTT17GENIChomozygous128096373
4157876756157876757GA34GENIChomozygous113400977
4157869342157869343CT24GENIChomozygous113563281