chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117516826117516827CG9GENIChomozygous115847407
7117518728117518729GA9GENIChomozygous115847417
7117520169117520170AG21GENIChomozygous115847419
7117521513117521514GC15GENIChomozygous115847421
7117521820117521821GA10GENIChomozygous115847423
7117521872117521873GA5GENIChomozygous115847425
7117523204117523205CT15GENIChomozygous115847427
7117524352117524353GA8GENIChomozygous115847429
7117526206117526207GA27GENIChomozygous115847431
7117526576117526577CT9GENIChomozygous115847433
7117526587117526588GA16GENIChomozygous115847435
7117526635117526636CT14GENIChomozygous115847437
7117526958117526959TC9GENIChomozygous115847439
7117528304117528305GA15GENIChomozygous115847441
7117528960117528961CT10GENIChomozygous115847443
7117529078117529079TG21GENIChomozygous115847445
7117529191117529192TC9GENIChomozygous115847447
7117529849117529850GT14GENIChomozygous115847451
7117533357117533358GA15GENIChomozygous115847453
7117534285117534286CT15GENIChomozygous115847455
7117537439117537440GA31GENIChomozygous115847457