chr start stop reference nuc variant nuc depth genic status zygosity variant ID 11 30880472 30880473 T C 26 GENIC homozygous 950629852 11 30880650 30880651 A G 11 GENIC homozygous 950629853 11 30881286 30881287 T C 23 GENIC homozygous 950629854 11 30882026 30882027 G A 9 GENIC homozygous 950629855 11 30883071 30883072 A G 15 GENIC homozygous 950629856 11 30883216 30883217 T C 10 GENIC homozygous 950629857 11 30884111 30884112 A G 19 GENIC homozygous 950629858 11 30884206 30884207 T C 9 GENIC homozygous 950629859 11 30884486 30884487 A G 19 GENIC homozygous 950629860 11 30886157 30886158 C T 16 GENIC homozygous 950629861 11 30886612 30886613 G C 13 GENIC homozygous 950629862 11 30886629 30886630 A G 12 GENIC homozygous 950629863 11 30886858 30886859 A G 27 GENIC homozygous 950629864 11 30887179 30887180 T C 10 GENIC homozygous 950629865 11 30887639 30887640 T C 27 GENIC homozygous 950629866 11 30889474 30889475 T C 14 GENIC homozygous 950629867 11 30889480 30889481 A G 13 GENIC homozygous 950629868 11 30890808 30890809 A G 13 GENIC homozygous 950629869 11 30890862 30890863 G A 11 GENIC homozygous 950629870 11 30891923 30891924 T A 12 GENIC homozygous 950629871