chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 108396131 108396132 A C 7 GENIC homozygous 116715794 10 108397121 108397122 A G 16 GENIC homozygous 116715796 10 108397668 108397669 C T 20 GENIC possibly homozygous 116715798 10 108398796 108398797 A T 13 GENIC homozygous 116715800 10 108399027 108399028 G A 21 GENIC homozygous 116715802 10 108399555 108399556 G C 20 GENIC homozygous 116715804 10 108399783 108399784 C T 25 GENIC homozygous 116715806 10 108400024 108400025 C T 15 GENIC homozygous 116715808 10 108400208 108400209 A G 17 GENIC homozygous 116715810 10 108401178 108401179 T C 20 GENIC homozygous 116715812 10 108401602 108401603 T C 10 GENIC homozygous 116715814 10 108401854 108401855 A T 16 GENIC homozygous 116715816 10 108401948 108401949 T C 9 GENIC homozygous 116715818 10 108402722 108402723 G A 8 GENIC homozygous 116715820 10 108403313 108403314 A C 5 GENIC homozygous 116715822 10 108407888 108407889 T C 25 GENIC homozygous 116715826 10 108407915 108407916 G T 19 GENIC homozygous 116715828 10 108409903 108409904 C A 12 GENIC homozygous 116715830 10 108404004 108404005 T C 2 GENIC homozygous 117261444 10 108404009 108404010 T C 4 GENIC heterozygous 117261446 10 108410467 108410468 A G 17 GENIC homozygous 116715832 10 108411514 108411515 C T 11 GENIC homozygous 116715834 10 108412793 108412794 G A 8 GENIC homozygous 116715836