chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1117948447117948448CA55GENIChomozygous135649824
1117949496117949497TC54GENIChomozygous135649828
1117950504117950505GA49GENIChomozygous135649833
1117954067117954068TC46GENIChomozygous135649844
1117958816117958817CT40GENIChomozygous142854403
1117950218117950219CT59GENIChomozygous141242004
1117956196117956197GA42GENIChomozygous142854401
1117958100117958101CT51GENIChomozygous142854402
1117959502117959503AG51GENIChomozygous135649857
1117961009117961010AT46GENIChomozygous135649858
1117961260117961261TC38GENIChomozygous135649859
1117961909117961910GA34GENIChomozygous135649860
1117962613117962614CA55GENIChomozygous135649862
1117962744117962745GA58GENIChomozygous135649863
1117963102117963103TC45GENIChomozygous135649864
1117963115117963116AC48GENIChomozygous135649865
1117963230117963231GT42GENIChomozygous135649866
1117963304117963305CT44GENIChomozygous135649867
1117963364117963365CG41GENIChomozygous135649868
1117963373117963374TA40GENIChomozygous135649869
1117963452117963453TC33GENIChomozygous135649870
1117963523117963524TC45GENIChomozygous135649871
1117963761117963762GA52GENIChomozygous142854404
1117963908117963909CT48GENIChomozygous135649872
1117963973117963974AG50GENIChomozygous135649873
1117963985117963986TC46GENIChomozygous135649874
1117951085117951086TC42GENICheterozygous403970843
1117951085117951086T42GENIChomozygous403970844
1117962624117962624AG57GENIChomozygous135424825
1117963405117963405G41GENIChomozygous135424826