chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8122382884122382885CT6GENIChomozygous116690213
8122382894122382895CT5GENIChomozygous116690215
8122382896122382897TC5GENIChomozygous116690217
8122383356122383357CT32GENICpossibly homozygous116690219
8122383721122383722CT27GENIChomozygous116690221
8122383786122383787TG22GENIChomozygous116690223
8122383799122383800TA20GENIChomozygous116690225
8122383862122383863TC26GENIChomozygous116690227
8122383923122383924GA25GENIChomozygous116690229
8122383936122383937GC24GENIChomozygous116690231
8122383984122383985CT24GENIChomozygous116690233
8122384064122384065GA27GENICpossibly homozygous116690235
8122384155122384156AC30GENIChomozygous116690237
8122384270122384271AT13GENIChomozygous116690239
8122384271122384272AG13GENIChomozygous116690241
8122384503122384504CT27GENIChomozygous116690247
8122384566122384567AC20GENIChomozygous116690249
8122384766122384767TC19GENIChomozygous116690251
8122384849122384850CT22GENIChomozygous116690253
8122384897122384898TC32GENIChomozygous116690255
8122384945122384946AT28GENIChomozygous117912805
8122385118122385119AG18GENIChomozygous116690257
8122385429122385430TC18GENIChomozygous116690261
8122385664122385665CT6GENIChomozygous116690263