chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 64789543 64789544 G A 50 GENIC homozygous 978995860 5 64790852 64790853 T C 25 GENIC homozygous 978995861 5 64791602 64791603 T A 28 GENIC homozygous 978995862 5 64793189 64793190 G C 21 GENIC homozygous 978995863 5 64794323 64794324 C T 11 GENIC homozygous 978995864 5 64794679 64794680 C T 16 GENIC homozygous 978995865 5 64794718 64794719 A G 16 GENIC homozygous 978995866 5 64795355 64795356 T C 49 GENIC homozygous 978995867 5 64795586 64795587 T G 13 GENIC homozygous 978995868 5 64795589 64795590 G T 11 GENIC homozygous 978995869 5 64795682 64795683 A G 17 GENIC homozygous 978995870 5 64795909 64795910 G A 16 GENIC homozygous 978995871 5 64796110 64796111 A G 9 GENIC homozygous 978995872 5 64796715 64796716 A G 39 GENIC homozygous 978995873 5 64796985 64796986 A G 18 GENIC homozygous 978995874 5 64799544 64799545 C T 43 GENIC homozygous 978995875 5 64799790 64799791 A G 29 GENIC homozygous 978995876 5 64800240 64800241 G C 30 GENIC homozygous 978995877