chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 39315304 39315305 T C 50 GENIC homozygous 510141928 12 39315612 39315613 G C 70 GENIC homozygous 508316489 12 39315737 39315738 G GTAT 57 GENIC homozygous 686245056 12 39317734 39317735 C T 54 GENIC homozygous 510141929 12 39317854 39317855 T C 62 GENIC homozygous 508316490 12 39319727 39319728 G GT 24 GENIC heterozygous 686245057 12 39321724 39321725 A G 38 GENIC homozygous 510141930 12 39321949 39321950 C T 56 GENIC homozygous 508316491 12 39322648 39322649 C G 31 GENIC homozygous 510141931 12 39322706 39322707 C T 25 GENIC heterozygous 510141932 12 39323213 39323214 T C 44 GENIC homozygous 508316492