chr start stop reference nuc variant nuc depth genic status zygosity variant ID 11 30727909 30727910 G A 61 GENIC homozygous 144093784 11 30729571 30729572 T 57 GENIC homozygous 141142734 11 30730221 30730222 G A 49 GENIC homozygous 144093785 11 30730222 30730223 G A 48 GENIC homozygous 144093786 11 30731393 30731394 T G 62 GENIC homozygous 138952912 11 30731608 30731609 T C 50 GENIC homozygous 138952913 11 30732021 30732022 C T 47 GENIC homozygous 138952914 11 30736930 30736931 T A 49 GENIC possibly homozygous 138952916 11 30737418 30737419 C T 42 GENIC homozygous 144093787 11 30737859 30737860 G A 57 GENIC homozygous 138952917 11 30738200 30738220 CGCGAGTGGGTATGTGCGCG 27 GENIC possibly homozygous 144090827 11 30738844 30738845 T A 63 GENIC homozygous 138952918 11 30738993 30738994 G 50 GENIC possibly homozygous 144090828 11 30739617 30739618 C T 50 GENIC homozygous 144093788 11 30739954 30739955 A T 61 GENIC homozygous 138952920 11 30740998 30740999 T G 61 GENIC homozygous 138952924 11 30741867 30741868 T C 53 GENIC possibly homozygous 144093789 11 30742025 30742026 A C 44 GENIC homozygous 138952925 11 30743448 30743449 G A 23 GENIC homozygous 144093790 11 30743472 30743473 G C 34 GENIC homozygous 138952931 11 30743826 30743827 A G 47 GENIC homozygous 138952932 11 30744133 30744134 T C 60 GENIC homozygous 144093791 11 30744149 30744150 C 55 GENIC homozygous 144090829 11 30745384 30745385 T C 55 GENIC homozygous 138952933 11 30745704 30745705 G A 61 GENIC homozygous 144093792 11 30748673 30748674 T C 63 GENIC homozygous 144093793