chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1227490813227490814CA16GENIChomozygous108559329
1227492779227492780TC21GENIChomozygous108559330
1227498589227498590GA14GENIChomozygous108559332
1227503016227503017TC4GENIChomozygous108559334
1227503026227503027AT6GENIChomozygous108559335
1227503203227503204CT26GENIChomozygous108559336
1227503499227503500TA9GENIChomozygous108559337
1227503925227503926AT6GENIChomozygous108559342
1227503945227503946CT8GENIChomozygous108559345
1227504021227504022GA10GENIChomozygous108559346
1227504124227504125AG6GENIChomozygous108559347
1227504127227504128CA5GENIChomozygous108559348
1227504214227504215CA9GENIChomozygous108559349
1227504245227504246TC15GENIChomozygous108559350
1227504308227504309TC14GENIChomozygous108559351
1227504582227504583CT6GENIChomozygous108559352
1227504747227504748GA5GENIChomozygous108559353
1227504748227504749CA4GENIChomozygous108559354
1227504750227504751GA5GENIChomozygous108559355
1227504760227504761TC6GENIChomozygous108559356
1227504761227504762TA6GENIChomozygous108559357
1227504907227504908CA10GENIChomozygous108559358
1227505024227505025AG13GENIChomozygous108559365
1227505052227505053GT15GENIChomozygous108559366
1227505375227505376TC13GENIChomozygous108559370
1227505591227505592AT7GENIChomozygous108559371
1227505617227505618CG10GENIChomozygous108559372
1227505680227505681TC22GENIChomozygous108559373
1227506153227506154AG12GENIChomozygous108559378
1227506333227506334CT7GENIChomozygous108559379
1227506336227506337CG7GENIChomozygous108559380
1227506441227506442CA15GENIChomozygous108559381