chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3110498358110498368CTTCTTCTTT10GENIChomozygous127918103
3110498369110498370AC10GENIChomozygous119702348
3110498374110498374C8GENIChomozygous127918104
3110498377110498378C8GENIChomozygous127918105
3110498397110498400ACA8GENIChomozygous127918106
3110498418110498419T9GENIChomozygous127918107
3110498421110498422CA7GENIChomozygous127988640
3110498423110498424G7GENIChomozygous127918108
3110498430110498431C9GENIChomozygous127918109
3110498441110498444CTG14GENIChomozygous127918110
3110498411110498412CT8GENIChomozygous132052029
3110499789110499790GA48GENIChomozygous111672865
3110503458110503459C17GENIChomozygous127918112
3110505507110505508TC47GENIChomozygous112003679
3110505750110505751CT68GENIChomozygous111672884
3110505866110505867TC58GENIChomozygous112003681
3110509767110509768GA49GENIChomozygous112003689
3110510216110510217AT54GENIChomozygous112003691
3110510613110510614GA44GENIChomozygous111672885
3110511887110511888AG62GENIChomozygous112003695
3110513094110513095CG68GENIChomozygous111672887
3110514954110514955GC57GENIChomozygous112003699
3110515246110515247GC58GENIChomozygous112003703
3110516979110516980TC56GENIChomozygous112003707
3110516650110516651CT51GENIChomozygous112138921
3110502928110502929C35GENICpossibly homozygous130907811
3110503504110503505TC31GENIChomozygous112138916
3110504763110504764AT56GENIChomozygous112138917
3110504969110504970GA62GENIChomozygous112138918
3110507116110507117GT51GENIChomozygous112138919
3110514906110514907GA56GENIChomozygous112138920