chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
96649683066496831AC14GENIChomozygous117369287
96649722666497227CT20GENIChomozygous117369289
96649738166497382TC19GENIChomozygous117369291
96649838966498390AT24GENIChomozygous117369293
96649853366498534CG22GENIChomozygous117369295
96649864766498648AG19GENIChomozygous117369296
96649977466499775TC13GENIChomozygous117369300
96650084666500847TC4GENIChomozygous117581555
96650093966500940AG17GENIChomozygous117369302
96650160966501610TC14GENIChomozygous117369304
96650162666501627AG17GENIChomozygous117369306
96650214366502144CA24GENIChomozygous117369308
96650327966503280CT19GENIChomozygous117369314
96650336466503365TA20GENIChomozygous117369316
96650345266503453TA24GENIChomozygous117369318
96650395866503959AG24GENIChomozygous117369320
96650597566505976TC10GENIChomozygous117369322
96650598066505981CG9GENIChomozygous117369324
96650627066506271GA14GENIChomozygous117369326
96650751466507515CT20GENIChomozygous117369330
96650753566507536CG18GENIChomozygous117369332
96650880766508808TC23GENIChomozygous117369334
96650918166509182AG16GENIChomozygous117369336
96650991366509914CT5GENIChomozygous117783348
96650993566509936AG7GENIChomozygous117783349
96651174866511749TG17GENIChomozygous117369338
96651183266511833GA19GENIChomozygous117369340
96651243266512433TG12GENIChomozygous117369342
96651337266513373AG29GENIChomozygous117369344
96651375366513754CA14GENIChomozygous117369346
96651510266515103AG14GENIChomozygous117369348
96651519366515194AG13GENIChomozygous117369350
96651632366516324AG20GENIChomozygous117369356
96651684966516850GA33GENIChomozygous117369358
96651698566516986TG22GENIChomozygous117369360
96651841466518415CA7GENIChomozygous117369362
96651890966518910GA14GENIChomozygous117369364
96652015766520158AG24GENIChomozygous117369366
96652039866520399CG17GENIChomozygous117369368
96652041466520415AG18GENIChomozygous117369370