chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7124024107124024108CT7GENIChomozygous116393955
7124024242124024243TC19GENIChomozygous116082717
7124025590124025591AG27GENIChomozygous115864596
7124026985124026986AC10GENIChomozygous115864598
7124027604124027605AG15GENICpossibly homozygous115864600
7124029142124029143TC18GENIChomozygous115864606
7124029635124029636AG21GENIChomozygous115864610
7124029662124029663TC25GENIChomozygous115864612
7124031212124031213CT13GENIChomozygous116082718
7124031511124031512TC14GENIChomozygous116082719
7124032149124032150GA11GENIChomozygous116082720
7124032681124032682TC14GENIChomozygous116082721
7124033252124033253CT17GENIChomozygous116082722
7124033398124033399GA13GENIChomozygous116082723
7124034146124034147GA16GENIChomozygous116082724
7124034674124034675GA13GENIChomozygous116082725
7124034868124034869AG15GENIChomozygous116082727
7124035483124035484TC19GENIChomozygous116082728
7124035542124035543AG18GENIChomozygous116082729
7124035612124035613AG20GENIChomozygous116082730
7124035639124035640CT14GENIChomozygous116393956
7124036144124036145GT21GENIChomozygous115864614
7124036353124036354TC20GENIChomozygous115864616
7124036622124036623GC31GENIChomozygous115864618
7124036671124036672AG27GENIChomozygous115864620
7124037131124037132TC23GENIChomozygous116082731
7124037439124037440GA25GENIChomozygous116082732
7124037519124037520AG28GENIChomozygous115864622
7124039001124039002AG17GENIChomozygous115864624
7124039678124039679GA18GENIChomozygous115864626
7124040712124040713TA29GENIChomozygous115864628
7124041071124041072AC24GENICheterozygous118454372
7124041414124041415AG14GENIChomozygous115864630