chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8122382884122382885CT37GENIChomozygous116690213
8122382894122382895CT35GENICpossibly homozygous116690215
8122382896122382897TC33GENIChomozygous116690217
8122383356122383357CT55GENIChomozygous116690219
8122383721122383722CT51GENIChomozygous116690221
8122383786122383787TG54GENIChomozygous116690223
8122383799122383800TA54GENIChomozygous116690225
8122383862122383863TC56GENIChomozygous116690227
8122383923122383924GA45GENIChomozygous116690229
8122383936122383937GC48GENIChomozygous116690231
8122383984122383985CT47GENIChomozygous116690233
8122384064122384065GA49GENIChomozygous116690235
8122384155122384156AC42GENIChomozygous116690237
8122384270122384271AT47GENIChomozygous116690239
8122384271122384272AG48GENIChomozygous116690241
8122384357122384358AG41GENIChomozygous116690243
8122384359122384360CT41GENIChomozygous116690245
8122384503122384504CT46GENIChomozygous116690247
8122384566122384567AC50GENIChomozygous116690249
8122384766122384767TC53GENIChomozygous116690251
8122384849122384850CT46GENIChomozygous116690253
8122384897122384898TC46GENIChomozygous116690255
8122385118122385119AG38GENIChomozygous116690257
8122385141122385142TC31GENIChomozygous116690259
8122385429122385430TC42GENIChomozygous116690261
8122385664122385665CT43GENIChomozygous116690263
8122385805122385806GA16GENIChomozygous116690265
8122386033122386034AG25GENIChomozygous116690267
8122397558122397559CT25GENIChomozygous116690269
8122397728122397729TC63GENICpossibly homozygous116690271
8122397902122397903TC50GENICpossibly homozygous116690273
8122398020122398021TC70GENICpossibly homozygous116690275
8122398098122398099TC52GENICheterozygous116690277