chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3107372857107372858TC17GENIChomozygous72074338
3107374964107374965TC29GENIChomozygous72074344
3107375816107375817G10GENIChomozygous73390455
3107375863107375864T16GENICheterozygous73390458
3107382270107382271TC17GENIChomozygous72074362
3107382432107382433TG7GENIChomozygous72074368
3107382489107382490GT18GENIChomozygous72074370
3107382514107382515T22GENICpossibly homozygous73390473
3107382532107382533TC16GENIChomozygous72074374
3107384188107384189TC19INTERGENIChomozygous72074386
3107400395107400396TC4INTERGENIChomozygous73750962
3107401793107401794GA12INTERGENIChomozygous73750964
3107377086107377086T17GENICheterozygous74211956
3107402099107402099A12GENICheterozygous74211959
3107393170107393171GA11INTERGENIChomozygous73628485
3107394102107394103C17INTERGENICheterozygous73628488
3107402129107402130AG12GENIChomozygous72074442
3107407481107407481A10GENIChomozygous74211962
3107415483107415484AG21GENIChomozygous72074478