chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1152786327152786328GC49GENIChomozygous135711332
1152786529152786530GC58GENIChomozygous141263462
1152786786152786787GA46GENIChomozygous135711333
1152786830152786831GA45GENIChomozygous141263463
1152787595152787596G15GENICheterozygous402968494
1152787595152787596GC15GENICheterozygous402968495
1152787597152787598G18GENICheterozygous402968496
1152787597152787598GC18GENICheterozygous402968497
1152789253152789254AC60GENICpossibly homozygous135711336
1152790306152790307GA59GENIChomozygous143792143
1152794355152794356AC49GENIChomozygous135711348
1152797080152797081AG44GENIChomozygous135711349
1152800631152800632AG46GENIChomozygous135711357
1152801073152801074GA51GENIChomozygous143792144
1152802543152802544TC21GENIChomozygous135711366
1152802909152802916AAAAAAG30GENIChomozygous135437799
1152797877152797877C37GENICpossibly homozygous143741637