chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1146715354146715355TG18GENIChomozygous108277940
1146715881146715882TC11GENIChomozygous108277942
1146717417146717418TG25GENIChomozygous108277944
1146719020146719021AG22GENIChomozygous108277946
1146721936146721937CA24GENIChomozygous108277948
1146725911146725912AG22GENIChomozygous108277952
1146726394146726395AG22GENIChomozygous108277954
1146726437146726438TC22GENIChomozygous108277956
1146726541146726542TG19GENIChomozygous108277958
1146727375146727376GA9GENIChomozygous108277960
1146727468146727469TC18GENIChomozygous108277962
1146727490146727491CT13GENIChomozygous108277964
1146727536146727537AG32GENIChomozygous108277966
1146728779146728780AC18GENIChomozygous108277974
1146728824146728825GA12GENIChomozygous125291816
1146728897146728898GC20GENIChomozygous125291817
1146729612146729613GA18GENIChomozygous108277980
1146731332146731333GA27GENIChomozygous108277982
1146731392146731393TC25GENIChomozygous108277984
1146731420146731421TC26GENIChomozygous108277986
1146731647146731648TC25GENIChomozygous108277988
1146731963146731964GA15GENIChomozygous108277990
1146732569146732570TC25GENIChomozygous108277992
1146733131146733132GA19GENIChomozygous108277994
1146733178146733179AG6GENICheterozygous125291818
1146733975146733976CT27GENIChomozygous108277996
1146734078146734079AG7GENIChomozygous108277998
1146734631146734632TC21GENIChomozygous108278000
1146735783146735784GA17GENIChomozygous108278002