chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 49889353 49889354 G GGTGTGTGTGTGTGTGTGT 1 GENIC homozygous 717067766 12 49890689 49890690 A AC 5 GENIC heterozygous 717067768 12 49891952 49891953 T C 18 GENIC homozygous 580014772 12 49892515 49892516 A G 18 GENIC homozygous 580014773 12 49892564 49892565 C CG 7 GENIC homozygous 717067769 12 49892994 49892995 A G 9 GENIC possibly homozygous 580014774 12 49893006 49893007 C T 12 GENIC homozygous 580014775 12 49893666 49893667 G A 18 GENIC possibly homozygous 580014776 12 49895907 49895908 A C 17 GENIC homozygous 580014777 12 49897028 49897029 G T 19 GENIC homozygous 580014778 12 49897105 49897106 G C 22 GENIC possibly homozygous 580014779 12 49899043 49899044 T C 18 GENIC homozygous 580014780 12 49900592 49900593 C T 18 GENIC possibly homozygous 580014781 12 49900691 49900692 G A 17 GENIC homozygous 580014782 12 49902577 49902578 G A 7 GENIC homozygous 580014783 12 49903130 49903131 C A 26 GENIC possibly homozygous 580014784 12 49905167 49905168 G A 15 GENIC homozygous 580014785 12 49907140 49907141 A T 6 GENIC heterozygous 580014786