chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 32303851 32303852 G A 17 GENIC homozygous 116790796 8 32304716 32304717 T C 26 GENIC homozygous 116790798 8 32306951 32306952 T C 38 GENIC homozygous 116790800 8 32307795 32307796 A G 21 GENIC homozygous 116448082 8 32308384 32308385 C G 21 GENIC homozygous 116790802 8 32308655 32308656 T C 28 GENIC homozygous 116448083 8 32309330 32309331 C T 27 GENIC homozygous 116790804 8 32311919 32311920 G A 30 GENIC homozygous 116790808 8 32311968 32311969 G A 29 GENIC homozygous 116790810 8 32315381 32315382 T C 28 GENIC possibly homozygous 116790812 8 32315623 32315624 G A 31 GENIC homozygous 116790814 8 32319606 32319607 C T 31 GENIC homozygous 116790816 8 32319876 32319877 T C 39 GENIC homozygous 116448087 8 32324116 32324117 T C 26 GENIC homozygous 116448088 8 32324657 32324658 T C 18 GENIC homozygous 116448089 8 32325228 32325229 A G 20 GENIC homozygous 116790820 8 32326291 32326292 C T 24 GENIC homozygous 116790822 8 32326575 32326576 A C 12 GENIC homozygous 116790824