chr start stop reference nuc variant nuc depth genic status zygosity variant ID 11 30880650 30880651 A G 43 GENIC homozygous 979969815 11 30880846 30880847 G A 38 GENIC homozygous 979969816 11 30881909 30881910 G A 60 GENIC homozygous 979969817 11 30883071 30883072 A G 15 GENIC homozygous 979969818 11 30883216 30883217 T C 40 GENIC homozygous 979969819 11 30884486 30884487 A G 15 GENIC homozygous 979969820 11 30886157 30886158 C T 60 GENIC homozygous 979969821 11 30886629 30886630 A G 33 GENIC homozygous 979969822 11 30887179 30887180 T C 86 GENIC homozygous 979969823 11 30888506 30888507 G A 38 GENIC homozygous 979969824 11 30889474 30889475 T C 60 GENIC homozygous 979969825 11 30889480 30889481 A G 61 GENIC homozygous 979969826 11 30891923 30891924 T A 9 GENIC homozygous 979969827 11 30892838 30892839 T C 21 GENIC homozygous 979969828