chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
113063001130630012CT25GENIChomozygous50715241
113063106930631070GA18GENICpossibly homozygous50715242
113063152830631529CT38GENICpossibly homozygous50715243
113063250630632507CG19GENICpossibly homozygous50715244
113063329530633296GA38GENICpossibly homozygous50715245
113063330630633307TC36GENIChomozygous50715246
113063369830633699AC22GENIChomozygous50715247
113063397430633980GTGTGT------4GENICheterozygous51195058
113063421430634215TC20GENIChomozygous50715249
113063465230634653AG32GENIChomozygous50715250
113063497230634973TC20GENIChomozygous50715251
113063559230635593CT23GENIChomozygous50715252
113063594130635942AC16GENIChomozygous50715253
113063655130636552AAAATTTTCTCT19GENIChomozygous50715254
113063671030636711TTCA22GENIChomozygous50715255
113063704530637046GA31GENIChomozygous50715256
113063764130637642AG24GENIChomozygous50715257
113063796430637965CT21GENIChomozygous50715258
113063810830638109GA24GENIChomozygous50715259
113063859630638597AG28GENIChomozygous50715260
113063898730638988GGAAAGAGCCAAACAAGGCCCTGCA34GENIChomozygous50715262
113063913930639140AG32GENIChomozygous50715263
113064009930640100AG30GENIChomozygous50715264
113064055830640559GA17GENIChomozygous50715265
113064079130640792CG12GENIChomozygous50715267
113064093630640937TTAACCACTGACTC13GENIChomozygous50715268
113063397230633980GTGTGTGT--------4GENICheterozygous51178431
113064068130640682AATAATAATAATAATAAT5GENIChomozygous51178433
113063475230634860AAAAAATATTACGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAGAACCAAAAAAAAA------------------------------------------------------------------------------------------------------------35GENIChomozygous51159501
113064161530641616TC16GENIChomozygous50715272
113064191330641914GC19GENIChomozygous50715273