chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46013549360135494A32GENICpossibly homozygous136886943
46013700260137003CA46GENIChomozygous137062265
46013908760139087CCT37GENIChomozygous136886944
46013934660139348GA29GENICheterozygous144347165
46014148960141490C47GENIChomozygous136886945
46014162260141623CT64GENIChomozygous137062266
46014173960141740TC50GENIChomozygous137062267
46014391860143919AT54GENIChomozygous137062268
46014442860144429CT55GENICpossibly homozygous137062269
46014454060144570TCTGTCTCTGTCTCTGTCTCTGTCTTTGTT11GENIChomozygous136886946
46014481760144818GA51GENIChomozygous137062270
46014657660146577AG46GENIChomozygous137062272
46014658060146581TG44GENIChomozygous137062273
46014689260146892TT9GENICheterozygous136886947
46014690660146907TG14GENIChomozygous137062274
46014717460147175GA32GENIChomozygous137062275
46014868460148684AA28GENIChomozygous136886948
46014943060149430A32GENIChomozygous136886949
46015208960152090TC49GENIChomozygous137062276
46015288660152887CT46GENIChomozygous137062277
46015436360154364GA54GENIChomozygous137062278
46015436460154365CG55GENIChomozygous137062279
46015514560155146AG37GENIChomozygous137062280
46015608160156082TC44GENIChomozygous137062281
46015627260156273TG44GENIChomozygous137062282
46015640160156402CT40GENIChomozygous137062283
46015641160156411G43GENIChomozygous136886950
46015660360156604AG58GENIChomozygous137062284
46015679860156798ATTC38GENIChomozygous136886951
46015722560157226GC44GENIChomozygous137062285
46015766560157666CT41GENIChomozygous137062286
46015952060159521AG36GENIChomozygous137062287
46016007860160079AG44GENIChomozygous137062288
46016299660162997CT48GENIChomozygous137062289
46016394760163951TACA18GENICheterozygous136886952
46016622460166225AT45GENIChomozygous137062290
46016770760167708AG25GENIChomozygous137062291
46017369460173695GA45GENIChomozygous137062292
46017377460173775TC36GENIChomozygous137062293
46017473860174739AC55GENIChomozygous137062294
46017749160177492TG47GENIChomozygous137062295