chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1117906845117906846TA250GENICheterozygous516208549
1117907037117907038CA250GENICheterozygous516208550
1117907180117907181TG250GENICheterozygous516208551
1117907189117907190TG250GENICheterozygous516208552
1117907307117907308GC250GENIChomozygous516208553
1117907332117907333TG250GENIChomozygous516208554
1117907365117907366AG249GENICheterozygous516208555
1117907422117907423AC249GENICheterozygous516208556
1117907495117907496CT247GENICheterozygous519202857
1117907944117907945AC247GENIChomozygous519202858
1117908015117908016TG35GENICpossibly homozygous519202859
1117908016117908017TA41GENIChomozygous519202860
1117908066117908067GT250GENICheterozygous516208557
1117908111117908112AG250GENIChomozygous519202861
1117908345117908346CG250GENICheterozygous519202862
1117908426117908427CT249GENICheterozygous516208558
1117908941117908942AT9GENIChomozygous516208559
1117908942117908943AC9GENIChomozygous516208560
1117909124117909125TA3GENICheterozygous519202863
1117909152117909153AAG3GENIChomozygous688517739
1117909197117909198AG102GENICheterozygous519202864
1117909211117909212TA119GENICheterozygous519202865
1117910846117910847CA16GENICheterozygous519202866
1117910937117910938GA34GENICheterozygous519202867