chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101456075214560753C-13GENICheterozygous51982655
101456789114567893GT--7GENICheterozygous52431617
101457569814575699TTG13GENICpossibly homozygous51329672
101458984914589850AATG3GENIChomozygous52356698
101459043114590432AG15GENIChomozygous51329676
101459107714591078AAT22GENIChomozygous51329677
101459130714591308CT26GENIChomozygous51329679
101459181714591818TC19GENIChomozygous51329680
101459202314592024CT21GENIChomozygous51329681
101459230314592307CACA----8GENIChomozygous52356700
101459399014593991AG22GENIChomozygous51329683
101459399214593994AC--23GENIChomozygous51329684
101459399514593996CA23GENIChomozygous51329685
101459407014594071AG21GENIChomozygous51329686
101459469614594697TC17GENIChomozygous51329688
101459513814595139GA31GENIChomozygous51329689
101459564814595649GA14GENIChomozygous51329690
101459692414596925GA26GENIChomozygous51329692
101459726014597261GT25GENIChomozygous51329693
101459762414597625CT38GENICpossibly homozygous51329695
101459770914597710CCTAACACAG34GENIChomozygous51329696
101459851114598513AA--16GENIChomozygous51329698
101460026014600261CT16GENIChomozygous51329699
101460143514601436CT23GENIChomozygous51329701
101460366514603666TC30GENIChomozygous51329702
101460372514603726TG22GENIChomozygous51329704
101460419614604197TTG5GENICheterozygous51329706