chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7108760952108760952G19GENIChomozygous137973470
7108761064108761065TC20GENIChomozygous145634354
7108762481108762482TC17GENIChomozygous145634355
7108763244108763245TC15GENIChomozygous145634356
7108763629108763630GC28GENIChomozygous145634357
7108763969108763970TC22GENIChomozygous145634358
7108764827108764828AT18GENIChomozygous145634359
7108766529108766529C19GENICpossibly homozygous145609935
7108766882108766883CT27GENIChomozygous145634360
7108766931108766932CT28GENIChomozygous145634361
7108767072108767073CT25GENIChomozygous145634362
7108766699108766700AG19GENIChomozygous138178405