chr start stop reference nuc variant nuc depth genic status zygosity variant ID 6 103762374 103762375 T C 32 GENIC homozygous 115144695 6 103762449 103762450 T A 73 GENIC possibly homozygous 115144696 6 103762464 103762465 G A 83 GENIC possibly homozygous 115144697 6 103762475 103762476 C G 85 GENIC heterozygous 115144698 6 103762535 103762536 G T 36 GENIC homozygous 115144699 6 103762613 103762614 C A 29 GENIC homozygous 115144700 6 103762734 103762735 C T 84 GENIC heterozygous 115144701 6 103762834 103762835 C T 42 GENIC heterozygous 115144702 6 103762948 103762949 G C 14 GENIC homozygous 115144703 6 103763050 103763051 C G 22 GENIC homozygous 115144705 6 103763059 103763060 C T 29 GENIC homozygous 115144706 6 103763198 103763199 C T 38 GENIC possibly homozygous 115144707 6 103763220 103763221 G A 44 GENIC possibly homozygous 115144708