chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 50362586 50362587 T C 11 GENIC homozygous 892657755 5 50362610 50362611 C T 5 GENIC heterozygous 892657756 5 50362700 50362701 T G 19 GENIC homozygous 892657757 5 50363116 50363117 C A 12 GENIC homozygous 892657758 5 50365354 50365355 G T 9 GENIC homozygous 892657759 5 50365355 50365356 A T 11 GENIC homozygous 892657760 5 50377405 50377406 G C 19 GENIC homozygous 892657761 5 50380622 50380623 G C 3 GENIC heterozygous 892657762 5 50382650 50382651 A T 8 GENIC homozygous 892657763 5 50382674 50382675 C T 13 GENIC homozygous 892657764 5 50383218 50383219 A G 5 GENIC homozygous 892657765 5 50383614 50383615 A G 10 GENIC homozygous 892657766 5 50389786 50389787 A G 14 GENIC homozygous 892657767 5 50390002 50390003 C G 12 GENIC homozygous 892657768 5 50390560 50390561 A T 11 GENIC homozygous 892657769 5 50392529 50392530 A G 13 GENIC homozygous 892657770 5 50392875 50392876 A G 13 GENIC homozygous 892657771