chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 103657968 103657969 A G 11 GENIC possibly homozygous 545928597 10 103658439 103658440 A G 14 GENIC homozygous 545928598 10 103658608 103658609 C T 12 GENIC possibly homozygous 547745693 10 103659475 103659476 A C 18 GENIC heterozygous 545928599 10 103660927 103660928 G A 14 GENIC homozygous 547745694 10 103661388 103661389 C G 21 GENIC homozygous 547745695 10 103662020 103662021 C T 12 GENIC homozygous 547745696 10 103662594 103662595 A G 9 GENIC homozygous 547745697 10 103663639 103663640 C T 25 GENIC homozygous 547745698 10 103664257 103664258 C T 15 GENIC possibly homozygous 547745699 10 103665617 103665618 C T 21 GENIC homozygous 547745700 10 103665767 103665768 A G 14 GENIC homozygous 545928600 10 103665802 103665803 C T 20 GENIC possibly homozygous 547745701 10 103666999 103667000 G A 11 GENIC possibly homozygous 547745702 10 103667623 103667624 C T 24 GENIC heterozygous 545928601 10 103667793 103667794 A G 13 GENIC heterozygous 545928602 10 103667854 103667855 A G 17 GENIC possibly homozygous 545928603 10 103668206 103668210 GTGT ---- 6 GENIC homozygous 698405761 10 103668953 103668954 C T 24 GENIC possibly homozygous 547745703 10 103669968 103669969 C T 14 GENIC homozygous 545928604 10 103670836 103670837 G A 5 GENIC homozygous 547745704