chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1216808988216808989TC19GENIChomozygous108536162
1216812966216812967AG17GENIChomozygous108536163
1216813465216813465A21GENIChomozygous130832779
1216816691216816691GGCAGTGGTGGGGTACCCCTTTAATCTCATCACTCAGAAAGCAGAGGCAGGCA19GENIChomozygous127483332
1216816772216816772A16GENIChomozygous127483333
1216821311216821311TGGCCA22GENIChomozygous127483334
1216822793216822793T20GENIChomozygous127483335
1216822801216822801AGAAAGAG20GENIChomozygous127483336
1216817931216817932GA20GENICpossibly homozygous120512002
1216823756216823756CAG8GENIChomozygous127483337
1216827857216827858TA4GENIChomozygous131796420
1216827849216827850TA4GENIChomozygous131796418
1216827851216827852TA4GENIChomozygous131796419
1216828240216828241AC13GENIChomozygous125408742
1216829210216829211CT21GENIChomozygous120512003