chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3107371510107371511CT17GENIChomozygous72445054
3107372115107372116T8GENICheterozygous74052410
3107372857107372858TC22GENIChomozygous72074338
3107374964107374965TC23GENICpossibly homozygous72074344
3107377086107377086T21GENICheterozygous74052413
3107381199107381200CT6GENIChomozygous72074352
3107382270107382271TC20GENIChomozygous72074362
3107382345107382346GT4GENIChomozygous72074364
3107382432107382433TG5GENIChomozygous72074368
3107382489107382490GT20GENIChomozygous72074370
3107382514107382515T20GENICpossibly homozygous73390473
3107375783107375784A9GENIChomozygous73527612
3107375816107375817G18GENIChomozygous73390455
3107375863107375864T11GENIChomozygous73390458
3107381158107381159T12GENIChomozygous73390469
3107382347107382348CT4GENIChomozygous73628482
3107382532107382533TC18GENIChomozygous72074374
3107384188107384189TC30INTERGENIChomozygous72074386
3107391683107391684GT8INTERGENIChomozygous73162559
3107391709107391710CT8INTERGENIChomozygous72074404
3107393196107393198TC5INTERGENIChomozygous73908176
3107397785107397786CA3INTERGENIChomozygous74052416
3107398010107398011CA17INTERGENIChomozygous72445067
3107402129107402130AG11GENIChomozygous72074442
3107405853107405854AC22GENICheterozygous72445082
3107408764107408765G26GENICheterozygous73908182
3107412950107412951TA20GENIChomozygous72445086
3107415216107415217CG6GENIChomozygous72445089
3107415483107415484AG19GENIChomozygous72074478