chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1117948447117948448CA44GENIChomozygous135649824
1117949496117949497TC38GENIChomozygous135649828
1117950136117950137AG47GENIChomozygous135649830
1117950504117950505GA55GENIChomozygous135649833
1117954067117954068TC39GENIChomozygous135649844
1117949191117949192CT52GENIChomozygous141242003
1117950218117950219CT49GENIChomozygous141242004
1117952576117952577GA39GENIChomozygous141242005
1117956447117956448CT43GENIChomozygous141242006
1117959200117959201CT39GENIChomozygous141242007
1117959328117959329CA42GENIChomozygous141242008
1117959502117959503AG39GENIChomozygous135649857
1117961260117961261TC42GENIChomozygous135649859
1117961909117961910GA56GENIChomozygous135649860
1117961951117961952GA59GENIChomozygous141242009
1117962023117962024GA65GENIChomozygous141242010
1117962056117962057CT60GENIChomozygous141242011
1117962613117962614CA62GENIChomozygous135649862
1117962624117962624AG61GENIChomozygous135424825
1117962744117962745GA60GENIChomozygous135649863
1117963102117963103TC50GENIChomozygous135649864
1117963115117963116AC46GENIChomozygous135649865
1117963230117963231GT42GENIChomozygous135649866
1117963304117963305CT45GENIChomozygous135649867
1117963364117963365CG40GENIChomozygous135649868
1117963373117963374TA39GENIChomozygous135649869
1117963405117963405G42GENIChomozygous135424826
1117963452117963453TC45GENIChomozygous135649870
1117963523117963524TC51GENIChomozygous135649871
1117963908117963909CT37GENIChomozygous135649872
1117963973117963974AG38GENIChomozygous135649873
1117963985117963986TC41GENIChomozygous135649874