chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10109972573109972574AAGTGTGTGT17GENIChomozygous51600694
10109972864109972865GGTTTT6GENIChomozygous51600695
10109973184109973185AG19GENIChomozygous51600697
10109973262109973263TA23GENIChomozygous51600698
10109973347109973348TC23GENIChomozygous51600699
10109973540109973541GA30GENIChomozygous51600700
10109974875109974880GTGTG-----38GENIChomozygous51600701
10109975491109975503ACACACACACAC------------6GENIChomozygous51600702
10109975533109975545AGAGAAAGAGAG------------17GENICheterozygous51600703
10109976247109976248GC13GENIChomozygous51600705
10109976380109976387TTGTTTG-------14GENICheterozygous51600708
10109976639109976640TC25GENIChomozygous51600710
10109976655109976656CT18GENIChomozygous51600711
10109976941109976942GA37GENIChomozygous51600712
10109977040109977044CACA----12GENICheterozygous51600713
10109977064109977065CT17GENICpossibly homozygous51600714
10109977462109977463GA14GENIChomozygous51600715
10109977776109977777CT31GENIChomozygous51600716
10109977804109977805GA27GENIChomozygous51958334
10109973421109973422CT25GENIChomozygous51958322
10109976379109976391TTTGTTTGTTTG------------7GENIChomozygous51958325
10109976678109976679CT18GENIChomozygous51958328
10109977023109977024CA20GENICpossibly homozygous51958331
10109979045109979046AG16GENIChomozygous51600719
10109979053109979054GGAACCC16GENIChomozygous51600720