chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1197311850197311852TG--20GENIChomozygous710756897
1197312336197312337T-4GENIChomozygous710756898
1197313171197313172AAT11GENIChomozygous710756899
1197313742197313743GA11GENIChomozygous571856979
1197314113197314114TTTC19GENICpossibly homozygous710756900
1197314113197314114TTAC19GENICheterozygous710756901
1197314179197314180AAG16GENICheterozygous710756902
1197314187197314191TGTT----15GENICheterozygous710756903
1197314401197314402GT29GENIChomozygous571856980
1197314402197314403GT30GENIChomozygous571856981
1197314409197314410GA34GENIChomozygous571856982
1197314724197314727AAA---9GENIChomozygous710756905
1197314784197314785AAG4GENIChomozygous710756906
1197314790197314801TATTTAAAGAA-----------4GENIChomozygous710756907
1197315092197315093GA21GENIChomozygous571856983