chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5134608228134608229GT24GENIChomozygous146142033
5134608602134608603CT15GENIChomozygous146142034
5134609067134609078TACCTACCCCC19GENIChomozygous146123334
5134609174134609175CT9GENIChomozygous146142035
5134609673134609674TA20GENIChomozygous146142036
5134611495134611496GT25GENIChomozygous146142037
5134612033134612034GT24GENIChomozygous146142038
5134612360134612361GT19GENIChomozygous146142039
5134613226134613227CG30GENIChomozygous146142040
5134614240134614241GT30GENIChomozygous146142041
5134615160134615161TC8GENIChomozygous137628292
5134615260134615260TTTGTTTTTATTTGTTTG21GENIChomozygous146123336
5134615826134615833CACACAC19GENIChomozygous146123337
5134615858134615879CAACACACACACACACAACAC19GENIChomozygous146123338
5134617635134617636A14GENIChomozygous146123341
5134619788134619789TC22GENIChomozygous137628298
5134619958134619959TC16GENIChomozygous137628299
5134622747134622748AG24GENIChomozygous137628300
5134617923134617923T17GENIChomozygous140884128
5134615860134615861A19GENIChomozygous403159126
5134615860134615861AC19GENICheterozygous403159127