chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7123963898123963899TC12GENICheterozygous115864452
7123965704123965705GA22GENIChomozygous115864454
7123968418123968419TG29GENIChomozygous115864456
7123968713123968714CT31GENIChomozygous115864458
7123969864123969865GA26GENIChomozygous115864460
7123971766123971767AG36GENIChomozygous115864462
7123974229123974230AT19GENIChomozygous115864464
7123974380123974381CT21GENIChomozygous115864466
7123975170123975171AG27GENIChomozygous115864468
7123975409123975410TC11GENIChomozygous115864470
7123976575123976576CA15GENICpossibly homozygous115864472
7123977293123977294AG38GENIChomozygous115864476
7123978290123978291CA17GENIChomozygous115864478
7123978704123978705AG34GENIChomozygous115864480
7123980437123980438GT13GENIChomozygous115864482
7123980595123980596AT17GENIChomozygous115864484
7123983263123983264CT29GENIChomozygous115864486
7123983467123983468GA28GENIChomozygous115864488
7123984015123984016AG26GENIChomozygous115864490
7123985372123985373TC28GENIChomozygous115864492
7123985393123985394GA31GENIChomozygous115864494
7123985915123985916CT33GENIChomozygous115864496
7123985976123985977GA31GENIChomozygous115864498
7123986923123986924TC31GENIChomozygous115864500
7123987196123987197CA22GENIChomozygous115864502
7123989685123989686CT47GENIChomozygous115864504
7123989792123989793AG42GENIChomozygous115864506
7123989818123989819TC39GENIChomozygous115864508
7123989872123989873CT36GENIChomozygous115864510