chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
153757018037570182GC17GENICheterozygous135359816
153760930137609302A6GENIChomozygous129246358
153763646237636464CG1GENIChomozygous129246361
153763957837639578TGGG5GENIChomozygous129246368
153763958037639580TTT8GENIChomozygous129246369
153763958137639581GCTCAGTGGT8GENIChomozygous129246370
153763958437639585AC11GENIChomozygous124064702
153763958437639584GCG10GENIChomozygous129246371
153763958937639589CTAGCAAGCA12GENIChomozygous129246372
153764421437644216AG16GENICheterozygous129246374
153760927537609276GC6GENIChomozygous112807899
153760932137609322TG5GENIChomozygous112807901