chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 83935697 83935698 G C 15 GENIC homozygous 108879754 1 83936269 83936270 C T 13 GENIC homozygous 108879755 1 83936415 83936416 C T 15 GENIC homozygous 108879756 1 83936803 83936804 G A 23 GENIC homozygous 108879757 1 83937964 83937965 A G 18 GENIC homozygous 109304939 1 83938700 83938701 A G 13 GENIC homozygous 120868661 1 83938730 83938731 A C 13 GENIC homozygous 108879758 1 83940022 83940023 G A 19 GENIC homozygous 108879759 1 83940193 83940194 T C 18 GENIC homozygous 108879760 1 83942980 83942981 G C 9 GENIC homozygous 108879762 1 83943690 83943691 A G 22 GENIC homozygous 108879763 1 83944101 83944102 G T 15 GENIC homozygous 108879764 1 83937963 83937964 G T 17 GENIC homozygous 120514118 1 83938413 83938414 G T 16 GENIC homozygous 120482416 1 83940545 83940546 T C 11 GENIC homozygous 120482417 1 83939795 83939797 AC 19 GENIC homozygous 131259042 1 83945166 83945167 T 18 GENIC homozygous 131259043