chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5144445236144445237CA7GENICheterozygous119223972
5144445624144445625CG8GENIChomozygous114037234
5144450137144450138AC17GENIChomozygous114037235
5144450220144450221AC16GENIChomozygous114037236
5144452978144452979GA15GENIChomozygous114037238
5144455293144455294GA3GENICheterozygous126205629
5144455542144455543CT22GENIChomozygous114037239
5144456187144456188CG13GENIChomozygous114037240
5144458353144458354AT17GENIChomozygous114037241
5144458908144458909GA16GENICheterozygous114037242
5144461574144461575TC15GENIChomozygous114037243
5144464288144464289GA8GENICheterozygous114037244
5144464635144464636GT10GENIChomozygous114037246
5144466382144466383GA22GENIChomozygous114037248
5144467856144467857TG23GENIChomozygous114037249
5144470469144470470TC13GENIChomozygous114037250
5144472792144472793TC9GENIChomozygous114037251
5144472796144472797AG7GENIChomozygous114037252
5144474035144474036CT16GENIChomozygous114037254
5144475025144475026GA16GENIChomozygous114037256
5144475284144475285CT15GENIChomozygous114037257
5144475934144475935AC14GENIChomozygous114037258
5144476260144476261TA15GENIChomozygous114037259
5144477140144477141CT16GENIChomozygous114037261
5144477623144477624TG14GENIChomozygous114037262
5144478110144478111AT15GENIChomozygous114037263
5144478190144478191AT17GENIChomozygous114037264
5144479062144479063TC6GENIChomozygous114037265