chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1146715354146715355TG24GENIChomozygous108277940
1146715881146715882TC25GENIChomozygous108277942
1146717417146717418TG19GENIChomozygous108277944
1146719020146719021AG22GENIChomozygous108277946
1146721936146721937CA27GENIChomozygous108277948
1146722923146722924AG36GENICpossibly homozygous108277950
1146725911146725912AG43GENIChomozygous108277952
1146726394146726395AG25GENIChomozygous108277954
1146726437146726438TC22GENIChomozygous108277956
1146726541146726542TG17GENIChomozygous108277958
1146727375146727376GA25GENIChomozygous108277960
1146727468146727469TC18GENIChomozygous108277962
1146727490146727491CT23GENIChomozygous108277964
1146727536146727537AG24GENIChomozygous108277966
1146727700146727701AC24GENIChomozygous108277968
1146728626146728627TA14GENIChomozygous108277970
1146728684146728685CA16GENIChomozygous108277972
1146728779146728780AC16GENIChomozygous108277974
1146729085146729086AG4GENIChomozygous108277976
1146729199146729200CG16GENIChomozygous108277978
1146729612146729613GA25GENICpossibly homozygous108277980
1146731332146731333GA22GENIChomozygous108277982
1146731392146731393TC22GENIChomozygous108277984
1146731420146731421TC26GENIChomozygous108277986
1146731647146731648TC26GENIChomozygous108277988
1146731963146731964GA25GENIChomozygous108277990
1146732569146732570TC25GENIChomozygous108277992
1146733131146733132GA26GENIChomozygous108277994
1146733975146733976CT19GENIChomozygous108277996
1146734078146734079AG26GENIChomozygous108277998
1146734631146734632TC20GENIChomozygous108278000
1146735783146735784GA18GENIChomozygous108278002