chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141761598617615987TC7GENIChomozygous948058350
141761819017618191AC38GENIChomozygous948058351
141761837217618373AC29GENIChomozygous948058352
141761868417618685TC27GENICpossibly homozygous948058353
141761936417619365TC17GENIChomozygous948058354
141761941517619416CG18GENIChomozygous948058355
141761943517619436CT15GENIChomozygous948058356
141761944417619445TC16GENIChomozygous948058357
141761952317619524CT15GENIChomozygous948058358
141762012717620128GA23GENIChomozygous948058359
141762023117620232CG23GENIChomozygous948058360
141762025317620254AG24GENIChomozygous948058361
141762138217621383TC29GENIChomozygous948058362
141762151417621515CT32GENIChomozygous948058363
141762256517622566TA13GENIChomozygous948058364
141762270917622710CT24GENIChomozygous948058365
141762355617623557AG26GENIChomozygous948058366
141762428217624283TA21GENIChomozygous948058367
141762439017624391TC20GENIChomozygous948058368
141762512217625123CG31GENIChomozygous948058369
141762520417625205TA32GENIChomozygous948058370
141762529517625296GA26GENIChomozygous948058371
141762557417625575CT18GENIChomozygous948058372
141762588517625886AG20GENIChomozygous948058373
141762834817628349GC19GENIChomozygous948058374
141762864117628642CT18GENIChomozygous948058375
141762944817629449AG15GENIChomozygous948058376
141762984117629842TC18GENIChomozygous948058377
141763004517630046GA29GENIChomozygous948058378
141763060517630606TA10GENIChomozygous948058379
141763098317630984TC23GENIChomozygous948058380
141763113017631131GA37GENIChomozygous948058381
141763137017631371AG34GENIChomozygous948058382