chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3107371510107371511CT12GENIChomozygous72445054
3107372857107372858TC11GENIChomozygous72074338
3107374964107374965TC17GENIChomozygous72074344
3107381199107381200CT9GENIChomozygous72074352
3107382270107382271TC8GENIChomozygous72074362
3107382432107382433TG5GENIChomozygous72074368
3107382489107382490GT14GENIChomozygous72074370
3107382514107382515T11GENICheterozygous73390473
3107375783107375784A10GENIChomozygous73527612
3107375816107375817G15GENIChomozygous73390455
3107375863107375864T13GENICheterozygous73390458
3107381158107381159T14GENICheterozygous73390469
3107377086107377086T16GENICheterozygous73908170
3107377908107377909CT4GENIChomozygous73908173
3107382532107382533TC10GENIChomozygous72074374
3107384188107384189TC18INTERGENIChomozygous72074386
3107393196107393198TC8INTERGENIChomozygous73908176
3107398010107398011CA12INTERGENIChomozygous72445067
3107402129107402130AG8GENIChomozygous72074442
3107405853107405854AC10GENIChomozygous72445082
3107407481107407481A11GENICheterozygous73908179
3107408764107408765G19GENICheterozygous73908182
3107412950107412951TA11GENIChomozygous72445086
3107415130107415130T4GENIChomozygous73908185
3107415483107415484AG10GENIChomozygous72074478
3107415216107415217CG10GENIChomozygous72445089