chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1104107924104107925GT11GENIChomozygous109422359
1104109406104109407TC12GENICpossibly homozygous108904495
1104110132104110133CT18GENIChomozygous108904499
1104110613104110614TG16GENIChomozygous109422361
1104115959104115960TG16GENICheterozygous108904502
1104115965104115966TG15GENICheterozygous109422363
1104116927104116928AT26GENICpossibly homozygous109422365
1104118027104118028TG14GENICpossibly homozygous108904507
1104119039104119040AG20GENIChomozygous108904511
1104126176104126177TC31GENIChomozygous109422367
1104127324104127325AC18GENIChomozygous109422369
1104128023104128024AG33GENIChomozygous108904533
1104130742104130743TC18GENIChomozygous108904546
1104130748104130749AG17GENIChomozygous108904547
1104132341104132342AG19GENIChomozygous108904554
1104132819104132820CT24GENIChomozygous109422371
1104133941104133942TC25GENIChomozygous108904555
1104134989104134990GA11GENIChomozygous109422373
1104135679104135680AG38GENICpossibly homozygous108904560
1104135931104135932GA23GENIChomozygous109422375
1104136545104136546AG30GENIChomozygous108904563
1104137195104137196TA24GENIChomozygous108904564
1104138008104138009CT15GENIChomozygous109422377
1104138563104138564CT18GENIChomozygous109422379
1104138974104138975AG17GENIChomozygous108904567
1104139175104139176CA23GENIChomozygous108904569
1104140125104140126GA19GENIChomozygous109422381
1104142508104142509GC32GENICpossibly homozygous108904593
1104142630104142631CT18GENIChomozygous108904596
1104143600104143601TA11GENIChomozygous109422383
1104143676104143677AG16GENIChomozygous108904604
1104143799104143800GA23GENIChomozygous108904605
1104143860104143861CA20GENIChomozygous108904607
1104144121104144122GA17GENIChomozygous108904608
1104144374104144375GA32GENIChomozygous109422385
1104144850104144851AT20GENIChomozygous109422387
1104144974104144975AG26GENIChomozygous109422389