chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
713259031325904CT22GENIChomozygous137987501
713259031325904C22GENICheterozygous403198243
713268471326848T16GENICheterozygous403198244
713268471326848TC16GENICheterozygous403198245
713268511326852T16GENICheterozygous403198246
713268511326852TG16GENICheterozygous403198247
713268521326853T16GENICheterozygous403198248
713268521326853TG16GENICheterozygous403198249
713269111326912AG17GENIChomozygous154435418
713287071328708GA23GENIChomozygous137987502
713291301329131GA5GENIChomozygous137987503
713331391333140AG15GENIChomozygous137987504
713340121334013T10GENICheterozygous403198250
713340121334013TA10GENIChomozygous403198251
713340141334015T10GENICheterozygous403198252
713340141334015TA10GENIChomozygous403198253
713340161334017T10GENICheterozygous403198254
713340161334017TA10GENIChomozygous403198255
713340181334019T10GENICheterozygous403198256
713340181334019TA10GENIChomozygous403198257
713341771334178CT7GENIChomozygous137987507
713344111334412GA9GENIChomozygous137987508
713349031334904CT16GENIChomozygous137987509
713359421335943AC19GENIChomozygous137987510
713363931336394GA17GENIChomozygous137987511
713367891336790CA22GENIChomozygous137987512
713372231337224GA17GENIChomozygous137987513
713394601339461CG22GENIChomozygous137987516
713398461339847CT23GENIChomozygous137987517
713291491329149A6GENICheterozygous144366812
713287611328761GGATCCCTT19GENIChomozygous137932494
713302771330277TG16GENIChomozygous137932495