chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 59897787 59897788 A G 17 GENIC homozygous 116608928 10 59899171 59899172 A G 19 GENIC homozygous 116789015 10 59899182 59899183 A G 20 GENIC homozygous 116789017 10 59899537 59899538 G T 30 GENIC homozygous 117995664 10 59899555 59899556 G A 36 GENIC homozygous 117995665 10 59899594 59899595 T C 23 GENIC homozygous 117995666 10 59899631 59899632 C T 20 GENIC homozygous 117995667 10 59899632 59899633 A G 20 GENIC homozygous 117995668 10 59899636 59899637 A G 21 GENIC homozygous 116608930 10 59899647 59899648 C T 24 GENIC homozygous 117142509 10 59899677 59899678 T C 30 GENIC homozygous 116608932 10 59899774 59899775 C T 41 GENIC heterozygous 118103932 10 59899822 59899823 C T 18 GENIC possibly homozygous 117995670 10 59899826 59899827 A C 18 GENIC possibly homozygous 117995671 10 59899827 59899828 A G 19 GENIC possibly homozygous 116608934 10 59900119 59900120 G A 21 GENIC homozygous 116608936 10 59900321 59900322 T G 21 GENIC homozygous 116608938 10 59902484 59902485 C T 22 GENIC homozygous 116608940 10 59902978 59902979 T C 26 GENIC homozygous 116608942 10 59903020 59903021 T C 20 GENIC homozygous 116608944 10 59905945 59905946 C T 32 GENIC homozygous 116789019 10 59909658 59909659 T C 7 GENIC homozygous 116608946 10 59899816 59899817 G C 25 GENIC possibly homozygous 117196108