chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 44186514 44186515 C T 19 GENIC homozygous 567537689 17 44187170 44187171 T C 18 GENIC homozygous 567537690 17 44187387 44187389 GT -- 1 GENIC homozygous 709299839 17 44187485 44187486 T A 25 GENIC homozygous 567537691 17 44188172 44188173 C T 18 GENIC homozygous 567537692 17 44188182 44188183 T C 17 GENIC homozygous 567537693 17 44188662 44188663 T C 20 GENIC homozygous 567537694 17 44189112 44189113 G - 13 GENIC homozygous 709299840 17 44189133 44189134 T A 12 GENIC homozygous 567537695 17 44189186 44189187 T C 1 GENIC homozygous 567537696 17 44189506 44189507 G A 8 GENIC homozygous 567537697 17 44189544 44189548 ACTT ---- 6 GENIC homozygous 709299842 17 44189566 44189567 C T 10 GENIC homozygous 567537698 17 44189759 44189763 AAAC ---- 7 GENIC homozygous 709299843 17 44189794 44189797 TGA --- 14 GENIC homozygous 709299844 17 44191373 44191374 C CT 14 GENIC possibly homozygous 709299845 17 44191846 44191847 G GGTGTGT 5 GENIC homozygous 709299850 17 44192019 44192020 T TC 14 GENIC homozygous 709299851