chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7129798708129798709CT10GENIChomozygous932548307
7129799658129799659GA11GENIChomozygous932548308
7129800613129800614CT12GENIChomozygous932548309
7129801117129801118AG8GENIChomozygous932548310
7129801936129801937GA6GENIChomozygous932548311
7129804694129804695TG11GENIChomozygous932548312
7129804776129804777TC12GENIChomozygous932548313
7129804821129804822GA9GENICpossibly homozygous932548314
7129805161129805162TC13GENIChomozygous932548315
7129805282129805283AG6GENIChomozygous932548316
7129805315129805316TC9GENIChomozygous932548317
7129805327129805328GT9GENIChomozygous932548318
7129806000129806001CT12GENIChomozygous932548319
7129806589129806590CT10GENIChomozygous932548320
7129807333129807334GA6GENIChomozygous932548321
7129807636129807637CA6GENIChomozygous932548322
7129808777129808778CT9GENIChomozygous932548323
7129808911129808912GT6GENIChomozygous932548324
7129808987129808988AG11GENIChomozygous932548325
7129810320129810321TC14GENIChomozygous932548326
7129810349129810350TC16GENIChomozygous932548327
7129810795129810796CT15GENIChomozygous932548328
7129810829129810830GA12GENIChomozygous932548329
7129811223129811224AG8GENIChomozygous932548330