chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
48852591888525919TC42GENIChomozygous119393101
48852604188526042GA61GENIChomozygous119393103
48852996188529962CA48GENIChomozygous112772699
48853065188530652CG63GENIChomozygous119393105
48853270288532703TC39GENIChomozygous112772706
48853310988533113GTTT47GENIChomozygous131355414
48853393688533937CG51GENICpossibly homozygous112772711
48853672788536728AG56GENIChomozygous112772718
48853809288538093GA46GENIChomozygous112772720
48854015988540160GC45GENIChomozygous112772729
48854035088540351GA42GENIChomozygous119393107
48854167288541673TC48GENIChomozygous119393109
48854259988542600CT50GENIChomozygous119393111
48854312088543121A56GENIChomozygous128057525
48854648188546482AG47GENICpossibly homozygous119393119
48854263588542636CT53GENIChomozygous119393113
48854375788543758AC41GENIChomozygous119393115
48854446188544462CT43GENIChomozygous119393117
48854535688545357CT54GENIChomozygous112772738
48854270188542702GC46GENIChomozygous132838133
48854654988546550TC71GENIChomozygous112772741
48854665888546659TC64GENIChomozygous112772742
48854671088546711AG44GENIChomozygous113041394
48854802288548023CA61GENIChomozygous112772743
48854865888548659GA48GENIChomozygous112772745
48855223088552231TG48GENIChomozygous112772748
48855290388552904TC39GENIChomozygous112772749
48855366288553663CT63GENIChomozygous119393121
48855527688555277GC34GENICpossibly homozygous112772755
48855631988556320GC50GENIChomozygous119393123
48856268688562687C46GENIChomozygous128057529
48856374588563746AC46GENIChomozygous113131202
48856447088564471CG11GENIChomozygous119435691