chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117516826117516827CG17GENIChomozygous115847407
7117518728117518729GA9GENIChomozygous115847417
7117520169117520170AG20GENIChomozygous115847419
7117521251117521252AG12GENIChomozygous126538386
7117521252117521253GT12GENIChomozygous126538387
7117521513117521514GC18GENIChomozygous115847421
7117521820117521821GA10GENIChomozygous115847423
7117521872117521873GA10GENIChomozygous115847425
7117523204117523205CT29GENIChomozygous115847427
7117524352117524353GA6GENIChomozygous115847429
7117526206117526207GA18GENIChomozygous115847431
7117526576117526577CT17GENIChomozygous115847433
7117526587117526588GA16GENIChomozygous115847435
7117526635117526636CT6GENIChomozygous115847437
7117526958117526959TC20GENIChomozygous115847439
7117528304117528305GA21GENIChomozygous115847441
7117528960117528961CT13GENIChomozygous115847443
7117529078117529079TG18GENIChomozygous115847445
7117529191117529192TC10GENIChomozygous115847447
7117529808117529809GA17GENIChomozygous115847449
7117529849117529850GT18GENIChomozygous115847451
7117533357117533358GA21GENIChomozygous115847453
7117534285117534286CT31GENIChomozygous115847455
7117537439117537440GA26GENIChomozygous115847457