chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 57606780 57606781 T C 30 GENIC homozygous 116604013 10 57607512 57607513 A G 30 GENIC homozygous 116604017 10 57607882 57607883 T C 33 GENIC homozygous 116604019 10 57608009 57608010 G C 28 GENIC homozygous 116604021 10 57608479 57608480 G C 24 GENIC homozygous 116604025 10 57608515 57608516 A G 26 GENIC homozygous 116604027 10 57609262 57609263 C T 35 GENIC homozygous 116604029 10 57609431 57609432 T C 26 GENIC homozygous 116604031 10 57610408 57610409 A G 33 GENIC homozygous 117060318 10 57610838 57610839 A G 27 GENIC homozygous 116604035 10 57611039 57611040 G A 36 GENIC possibly homozygous 116604039 10 57611545 57611546 T C 17 GENIC homozygous 116785601 10 57612449 57612450 C T 41 GENIC homozygous 116785603 10 57613496 57613497 G A 24 GENIC homozygous 116785605