chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7124024107124024108CT13GENIChomozygous116393955
7124024242124024243TC15GENIChomozygous116082717
7124025590124025591AG14GENIChomozygous115864596
7124026985124026986AC10GENIChomozygous115864598
7124027604124027605AG13GENIChomozygous115864600
7124029142124029143TC9GENIChomozygous115864606
7124029635124029636AG12GENIChomozygous115864610
7124029662124029663TC14GENIChomozygous115864612
7124031212124031213CT11GENIChomozygous116082718
7124031511124031512TC12GENIChomozygous116082719
7124032149124032150GA12GENIChomozygous116082720
7124032681124032682TC18GENIChomozygous116082721
7124033252124033253CT10GENIChomozygous116082722
7124033398124033399GA16GENIChomozygous116082723
7124034146124034147GA10GENIChomozygous116082724
7124034674124034675GA6GENIChomozygous116082725
7124034868124034869AG17GENIChomozygous116082727
7124035379124035380AC10GENIChomozygous126620201
7124035483124035484TC15GENIChomozygous116082728
7124035542124035543AG15GENIChomozygous116082729
7124035612124035613AG12GENIChomozygous116082730
7124035639124035640CT14GENIChomozygous116393956
7124036144124036145GT15GENIChomozygous115864614
7124036353124036354TC15GENIChomozygous115864616
7124036622124036623GC14GENIChomozygous115864618
7124036671124036672AG13GENIChomozygous115864620
7124037131124037132TC16GENIChomozygous116082731
7124037439124037440GA11GENIChomozygous116082732
7124037519124037520AG10GENIChomozygous115864622
7124028097124028097G4GENIChomozygous131874673
7124034638124034638C7GENIChomozygous131874674
7124035375124035376G10GENIChomozygous131874675
7124036004124036004T14GENIChomozygous131874676
7124039001124039002AG16GENIChomozygous115864624
7124039678124039679GA13GENIChomozygous115864626
7124040677124040678A10GENIChomozygous128514196
7124040712124040713TA13GENIChomozygous115864628
7124041414124041415AG7GENIChomozygous115864630