chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8122382884122382885CT18GENIChomozygous116690213
8122382894122382895CT17GENIChomozygous116690215
8122382896122382897TC16GENIChomozygous116690217
8122383356122383357CT18GENIChomozygous116690219
8122383721122383722CT21GENIChomozygous116690221
8122383786122383787TG18GENIChomozygous116690223
8122383799122383800TA18GENIChomozygous116690225
8122383862122383863TC25GENIChomozygous116690227
8122383923122383924GA24GENIChomozygous116690229
8122383936122383937GC20GENIChomozygous116690231
8122383984122383985CT22GENIChomozygous116690233
8122384064122384065GA25GENIChomozygous116690235
8122384155122384156AC22GENIChomozygous116690237
8122384204122384205AC17GENIChomozygous116895093
8122384270122384271AT19GENIChomozygous116690239
8122384271122384272AG19GENIChomozygous116690241
8122384357122384358AG24GENIChomozygous116690243
8122384359122384360CT24GENIChomozygous116690245
8122384503122384504CT22GENIChomozygous116690247
8122384566122384567AC18GENIChomozygous116690249
8122384766122384767TC29GENIChomozygous116690251
8122384849122384850CT30GENIChomozygous116690253
8122384897122384898TC28GENIChomozygous116690255
8122385118122385119AG18GENIChomozygous116690257
8122385141122385142TC15GENIChomozygous116690259
8122385429122385430TC22GENIChomozygous116690261
8122385664122385665CT12GENIChomozygous116690263
8122385805122385806GA7GENICpossibly homozygous116690265
8122386033122386034AG21GENIChomozygous116690267
8122397558122397559CT10GENIChomozygous116690269
8122397728122397729TC24GENIChomozygous116690271
8122397902122397903TC47GENICpossibly homozygous116690273
8122398020122398021TC54GENICpossibly homozygous116690275
8122398098122398099TC36GENICheterozygous116690277
8122397907122397908TA45GENICheterozygous116988355