chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1101501813101501815CA--6GENICheterozygous747965343
1101502067101502069AC--13GENICheterozygous747965345
1101503217101503219AC--3GENICheterozygous747965349
1101509496101509500TCTG----26GENICheterozygous747965350
1101514513101514515GT--12GENICheterozygous747965352
1101519882101519884AC--17GENICheterozygous747965353
1101520725101520727TG--5GENICheterozygous747965355
1101523388101523389TTG29GENIChomozygous747965356
1101524774101524776GT--10GENICheterozygous747965357
1101525080101525082TG--26GENICheterozygous747965359
1101529570101529572GA--18GENICheterozygous747965361
1101534258101534259A-14GENICheterozygous747965365
1101534285101534286A-19GENICheterozygous747965366