chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7108760952108760952G43GENIChomozygous137973470
7108761064108761065TC42GENIChomozygous145634354
7108762481108762482TC43GENIChomozygous145634355
7108763244108763245TC37GENIChomozygous145634356
7108763629108763630GC37GENIChomozygous145634357
7108763969108763970TC46GENIChomozygous145634358
7108764827108764828AT28GENICpossibly homozygous145634359
7108766529108766529C25GENIChomozygous145609935
7108766699108766700AG37GENIChomozygous138178405
7108766882108766883CT31GENIChomozygous145634360
7108766931108766932CT31GENIChomozygous145634361
7108767072108767073CT38GENIChomozygous145634362