chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 44186514 44186515 C T 46 GENIC homozygous 503697768 17 44187170 44187171 T C 24 GENIC homozygous 503697769 17 44187379 44187383 GTGT ---- 5 GENIC heterozygous 684826961 17 44187381 44187383 GT -- 5 GENIC heterozygous 684826962 17 44187485 44187486 T A 38 GENIC homozygous 503697770 17 44188172 44188173 C T 58 GENIC homozygous 503697771 17 44188182 44188183 T C 50 GENIC homozygous 503697772 17 44188662 44188663 T C 35 GENIC homozygous 503697773 17 44189112 44189113 G - 25 GENIC homozygous 684826964 17 44189133 44189134 T A 32 GENIC homozygous 503697774 17 44189186 44189187 T C 26 GENIC homozygous 503697775 17 44189506 44189507 G A 20 GENIC homozygous 503697776 17 44189544 44189548 ACTT ---- 13 GENIC homozygous 684826965 17 44189566 44189567 C T 21 GENIC homozygous 503697777 17 44189759 44189763 AAAC ---- 33 GENIC homozygous 684826966 17 44189794 44189797 TGA --- 27 GENIC homozygous 684826967 17 44191229 44191230 C G 35 GENIC heterozygous 503697778 17 44191373 44191374 C CT 27 GENIC homozygous 684826968 17 44192019 44192020 T TC 34 GENIC homozygous 684826969 17 44192086 44192087 C T 30 GENIC heterozygous 503697779 17 44192614 44192615 A G 27 GENIC homozygous 503697780