chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 173340455 173340456 A G 24 GENIC possibly homozygous 807631466 5 173341068 173341069 C T 64 GENIC homozygous 807631467 5 173342937 173342938 G C 49 GENIC homozygous 807631468 5 173344718 173344719 C T 49 GENIC possibly homozygous 807631469 5 173345388 173345389 G A 51 GENIC homozygous 807631470 5 173345461 173345462 G A 45 GENIC possibly homozygous 807631471 5 173345467 173345468 G A 46 GENIC possibly homozygous 807631472 5 173345503 173345504 C T 32 GENIC homozygous 807631473 5 173347147 173347148 A G 44 GENIC homozygous 807631474 5 173347178 173347179 T C 47 GENIC homozygous 807631475 5 173347309 173347310 T A 45 GENIC possibly homozygous 807631476 5 173347489 173347490 T C 50 GENIC homozygous 807631477 5 173347683 173347684 A G 41 GENIC homozygous 807631478 5 173348062 173348063 G T 42 GENIC homozygous 807631479 5 173348303 173348304 G A 58 GENIC homozygous 807631480 5 173348372 173348373 A G 50 GENIC homozygous 807631481 5 173348932 173348933 G A 46 GENIC homozygous 807631482 5 173349421 173349422 T A 60 GENIC homozygous 807631483 5 173349703 173349704 A G 44 GENIC homozygous 807631484 5 173349906 173349907 A C 53 GENIC homozygous 807631485 5 173350381 173350382 T C 29 GENIC homozygous 807631486 5 173350440 173350441 G A 48 GENIC homozygous 807631487 5 173352655 173352656 C T 40 GENIC homozygous 807631488 5 173352692 173352693 A G 40 GENIC homozygous 807631489 5 173352901 173352902 T C 47 GENIC possibly homozygous 807631490 5 173354070 173354071 G A 39 GENIC possibly homozygous 807631491