chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117516826117516827CG40GENICpossibly homozygous115847407
7117518639117518640GC113GENICheterozygous115847409
7117518728117518729GA29GENICpossibly homozygous115847417
7117520169117520170AG51GENICpossibly homozygous115847419
7117521513117521514GC51GENIChomozygous115847421
7117521820117521821GA45GENIChomozygous115847423
7117521872117521873GA34GENIChomozygous115847425
7117523204117523205CT29GENIChomozygous115847427
7117523219117523220TG17GENICheterozygous116393568
7117524352117524353GA50GENIChomozygous115847429
7117526206117526207GA46GENIChomozygous115847431
7117526576117526577CT57GENICpossibly homozygous115847433
7117526587117526588GA52GENIChomozygous115847435
7117526635117526636CT38GENIChomozygous115847437
7117526958117526959TC37GENIChomozygous115847439
7117528304117528305GA50GENIChomozygous115847441
7117528960117528961CT36GENICpossibly homozygous115847443
7117529078117529079TG71GENIChomozygous115847445
7117529191117529192TC56GENIChomozygous115847447
7117529808117529809GA40GENIChomozygous115847449
7117529849117529850GT49GENICpossibly homozygous115847451
7117533357117533358GA53GENIChomozygous115847453
7117534285117534286CT46GENICpossibly homozygous115847455
7117537439117537440GA60GENIChomozygous115847457