chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117516826117516827CG14GENIChomozygous115847407
7117517206117517218GGGGGTGGAGGC14GENIChomozygous128510589
7117518065117518065C14GENIChomozygous128510590
7117518660117518662AC20GENIChomozygous128510591
7117518690117518692AG17GENICheterozygous128510592
7117520169117520170AG14GENIChomozygous115847419
7117521251117521252A20GENIChomozygous128510593
7117521513117521514GC33GENIChomozygous115847421
7117521820117521821GA21GENIChomozygous115847423
7117521872117521873GA24GENIChomozygous115847425
7117523204117523205CT23GENIChomozygous115847427
7117524352117524353GA25GENIChomozygous115847429
7117525291117525295CCGG23GENIChomozygous128510594
7117526206117526207GA22GENIChomozygous115847431
7117526539117526539A26GENIChomozygous128510595
7117526576117526577CT28GENIChomozygous115847433
7117528304117528305GA31GENIChomozygous115847441
7117526587117526588GA26GENIChomozygous115847435
7117526635117526636CT30GENIChomozygous115847437
7117526958117526959TC25GENIChomozygous115847439
7117528960117528961CT25GENIChomozygous115847443
7117529078117529079TG22GENIChomozygous115847445
7117529191117529192TC25GENIChomozygous115847447
7117529808117529809GA23GENIChomozygous115847449
7117529849117529850GT25GENIChomozygous115847451
7117533357117533358GA28GENIChomozygous115847453
7117534285117534286CT19GENIChomozygous115847455
7117537439117537440GA25GENIChomozygous115847457