chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 44186514 44186515 C T 18 GENIC possibly homozygous 577325764 17 44187170 44187171 T C 22 GENIC homozygous 577325765 17 44187385 44187389 GTGT ---- 3 GENIC heterozygous 715555912 17 44187387 44187389 GT -- 3 GENIC heterozygous 715555913 17 44187485 44187486 T A 18 GENIC homozygous 577325766 17 44188172 44188173 C T 17 GENIC homozygous 577325767 17 44188182 44188183 T C 18 GENIC homozygous 577325768 17 44188662 44188663 T C 23 GENIC homozygous 577325769 17 44189112 44189113 G - 13 GENIC homozygous 715555914 17 44189133 44189134 T A 14 GENIC homozygous 577325770 17 44189186 44189187 T C 8 GENIC homozygous 577325771 17 44189506 44189507 G A 15 GENIC homozygous 577325772 17 44189544 44189548 ACTT ---- 19 GENIC homozygous 715555916 17 44189566 44189567 C T 22 GENIC homozygous 577325773 17 44189759 44189763 AAAC ---- 11 GENIC homozygous 715555917 17 44189794 44189797 TGA --- 12 GENIC homozygous 715555918 17 44191373 44191374 C CT 13 GENIC possibly homozygous 715555919 17 44191846 44191847 G GGTGTGT 1 GENIC homozygous 715555924 17 44192019 44192020 T TC 20 GENIC homozygous 715555925