chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
55723053257230533GC22GENIChomozygous137476373
55723349757233498TC34GENICpossibly homozygous137476374
55723369557233696AT47GENIChomozygous137476375
55723402457234025CA48GENIChomozygous137476376
55723538357235384GA43GENIChomozygous137476377
55723600457236005TC44GENIChomozygous137476378
55723706257237063TC50GENIChomozygous137476379
55723730257237303GA51GENIChomozygous137476380
55723745957237460CG43GENIChomozygous137476381
55723787757237878TC43GENIChomozygous137476382
55723869457238695AG27GENIChomozygous137476383
55723942857239429CT36GENIChomozygous137476384
55723943057239431AG36GENIChomozygous137476385
55723511357235116TCT43GENIChomozygous137310140
55723104457231044CTGT53GENIChomozygous137310138
55723223757232241AGGA19GENIChomozygous137310139