chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 173341068 173341069 C T 28 GENIC homozygous 952487394 5 173342937 173342938 G C 12 GENIC homozygous 952487395 5 173344718 173344719 C T 30 GENIC homozygous 952487396 5 173345388 173345389 G A 24 GENIC homozygous 952487397 5 173345461 173345462 G A 14 GENIC homozygous 952487398 5 173345467 173345468 G A 17 GENIC homozygous 952487399 5 173345503 173345504 C T 11 GENIC homozygous 952487400 5 173347147 173347148 A G 15 GENIC homozygous 952487401 5 173347178 173347179 T C 18 GENIC homozygous 952487402 5 173347309 173347310 T A 29 GENIC homozygous 952487403 5 173347489 173347490 T C 29 GENIC homozygous 952487404 5 173347683 173347684 A G 20 GENIC homozygous 952487405 5 173348062 173348063 G T 16 GENIC homozygous 952487406 5 173348303 173348304 G A 22 GENIC homozygous 952487407 5 173348372 173348373 A G 26 GENIC homozygous 952487408 5 173348932 173348933 G A 26 GENIC homozygous 952487409 5 173349421 173349422 T A 35 GENIC homozygous 952487410 5 173349703 173349704 A G 21 GENIC homozygous 952487411 5 173349906 173349907 A C 31 GENIC homozygous 952487412 5 173350440 173350441 G A 26 GENIC homozygous 952487413 5 173352655 173352656 C T 26 GENIC homozygous 952487414 5 173352901 173352902 T C 32 GENIC homozygous 952487415 5 173354070 173354071 G A 19 GENIC homozygous 952487416