chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
96649683066496831AC29GENIChomozygous117369287
96649722666497227CT28GENIChomozygous117369289
96649738166497382TC22GENIChomozygous117369291
96649838966498390AT26GENIChomozygous117369293
96649853366498534CG31GENIChomozygous117369295
96649864766498648AG30GENIChomozygous117369296
96649977466499775TC13GENIChomozygous117369300
96650084666500847TC12GENIChomozygous117581555
96650093966500940AG23GENIChomozygous117369302
96650160966501610TC16GENIChomozygous117369304
96650162666501627AG17GENIChomozygous117369306
96650214366502144CA18GENIChomozygous117369308
96650327966503280CT22GENIChomozygous117369314
96650336466503365TA25GENIChomozygous117369316
96650345266503453TA23GENIChomozygous117369318
96650395866503959AG23GENIChomozygous117369320
96650597566505976TC17GENIChomozygous117369322
96650598066505981CG15GENIChomozygous117369324
96650627066506271GA17GENIChomozygous117369326
96650751466507515CT26GENIChomozygous117369330
96650753566507536CG19GENIChomozygous117369332
96650880766508808TC27GENIChomozygous117369334
96650918166509182AG14GENIChomozygous117369336
96650991366509914CT2GENIChomozygous117783348
96650993566509936AG3GENIChomozygous117783349
96651174866511749TG20GENIChomozygous117369338
96651183266511833GA17GENIChomozygous117369340
96651243266512433TG13GENIChomozygous117369342
96651337266513373AG31GENIChomozygous117369344
96651375366513754CA21GENIChomozygous117369346
96651510266515103AG31GENIChomozygous117369348
96651519366515194AG17GENIChomozygous117369350
96651632366516324AG40GENIChomozygous117369356
96651684966516850GA24GENIChomozygous117369358
96651698566516986TG26GENIChomozygous117369360
96651841466518415CA11GENIChomozygous117369362
96651890966518910GA16GENIChomozygous117369364
96652015766520158AG23GENIChomozygous117369366
96652039866520399CG23GENIChomozygous117369368
96652041466520415AG21GENIChomozygous117369370