chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 8983559 8983560 C T 27 GENIC homozygous 972114874 3 8983625 8983626 C G 23 GENIC homozygous 972114875 3 8984305 8984306 T A 19 GENIC homozygous 972114876 3 8984423 8984424 A G 18 GENIC homozygous 972114877 3 8985027 8985028 A G 26 GENIC homozygous 972114878 3 8985588 8985589 G T 16 GENIC homozygous 972114879 3 8986032 8986033 G T 21 GENIC homozygous 972114880 3 8987027 8987028 G C 13 GENIC homozygous 972114881 3 8989345 8989346 T C 13 GENIC homozygous 972114882 3 8992378 8992379 A G 27 GENIC homozygous 972114883 3 8992637 8992638 A G 38 GENIC homozygous 972114884 3 8992828 8992829 T C 36 GENIC homozygous 972114885 3 8997340 8997341 A G 24 GENIC homozygous 972114886 3 8999098 8999099 G C 21 GENIC possibly homozygous 972114887 3 9003899 9003900 G C 23 GENIC homozygous 972114888 3 9004788 9004789 A G 27 GENIC homozygous 972114889 3 9005197 9005198 C T 32 GENIC homozygous 972114890 3 9005627 9005628 G A 49 GENIC homozygous 972114891 3 9006532 9006533 T C 31 GENIC homozygous 972114892 3 9009522 9009523 T C 19 GENIC homozygous 972114893 3 9009628 9009629 T C 23 GENIC homozygous 972114894