chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 173341068 173341069 C T 32 GENIC homozygous 943981600 5 173342937 173342938 G C 27 GENIC homozygous 943981601 5 173344718 173344719 C T 26 GENIC homozygous 943981602 5 173345388 173345389 G A 25 GENIC homozygous 943981603 5 173345461 173345462 G A 28 GENIC homozygous 943981604 5 173345503 173345504 C T 21 GENIC homozygous 943981605 5 173347147 173347148 A G 36 GENIC homozygous 943981606 5 173347178 173347179 T C 31 GENIC homozygous 943981607 5 173347309 173347310 T A 42 GENIC homozygous 943981608 5 173347489 173347490 T C 29 GENIC homozygous 943981609 5 173347683 173347684 A G 25 GENIC homozygous 943981610 5 173348062 173348063 G T 30 GENIC homozygous 943981611 5 173348303 173348304 G A 33 GENIC homozygous 943981612 5 173348372 173348373 A G 42 GENIC homozygous 943981613 5 173348932 173348933 G A 24 GENIC homozygous 943981614 5 173349421 173349422 T A 18 GENIC homozygous 943981615 5 173349703 173349704 A G 38 GENIC homozygous 943981616 5 173349906 173349907 A C 26 GENIC homozygous 943981617 5 173350381 173350382 T C 15 GENIC homozygous 943981618 5 173350440 173350441 G A 16 GENIC homozygous 943981619 5 173352655 173352656 C T 29 GENIC homozygous 943981620 5 173352692 173352693 A G 22 GENIC homozygous 943981621 5 173352901 173352902 T C 31 GENIC homozygous 943981622 5 173354070 173354071 G A 13 GENIC homozygous 943981623