chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117516826117516827CG49GENIChomozygous115847407
7117517206117517218GGGGGTGGAGGC11GENIChomozygous128510589
7117518065117518065C43GENICpossibly homozygous128510590
7117518660117518662AC26GENICheterozygous128510591
7117518690117518692AG17GENICheterozygous128510592
7117520169117520170AG42GENIChomozygous115847419
7117521513117521514GC46GENIChomozygous115847421
7117521820117521821GA57GENIChomozygous115847423
7117521872117521873GA59GENIChomozygous115847425
7117523204117523205CT41GENIChomozygous115847427
7117524352117524353GA50GENIChomozygous115847429
7117526587117526588GA37GENIChomozygous115847435
7117521251117521252A31GENIChomozygous128510593
7117525291117525295CCGG49GENIChomozygous128510594
7117526539117526539A40GENIChomozygous128510595
7117526206117526207GA46GENIChomozygous115847431
7117526576117526577CT39GENIChomozygous115847433
7117526635117526636CT35GENICpossibly homozygous115847437
7117526958117526959TC47GENIChomozygous115847439
7117528304117528305GA43GENIChomozygous115847441
7117528960117528961CT48GENIChomozygous115847443
7117529078117529079TG51GENIChomozygous115847445
7117529191117529192TC56GENIChomozygous115847447
7117529808117529809GA51GENIChomozygous115847449
7117529849117529850GT51GENIChomozygous115847451
7117533357117533358GA48GENIChomozygous115847453
7117534285117534286CT47GENIChomozygous115847455
7117537439117537440GA63GENIChomozygous115847457