chr start stop reference nuc variant nuc depth genic status zygosity variant ID 11 30880650 30880651 A G 12 GENIC homozygous 958868180 11 30881150 30881151 C T 33 GENIC homozygous 958868181 11 30881388 30881389 T C 18 GENIC homozygous 958868182 11 30883216 30883217 T C 17 GENIC homozygous 958868183 11 30883314 30883315 G C 32 GENIC homozygous 958868184 11 30884486 30884487 A G 13 GENIC homozygous 958868185 11 30885831 30885832 C T 21 GENIC homozygous 958868186 11 30886157 30886158 C T 25 GENIC homozygous 958868187 11 30886629 30886630 A G 17 GENIC homozygous 958868188 11 30886795 30886796 T C 21 GENIC homozygous 958868189 11 30887179 30887180 T C 29 GENIC homozygous 958868190 11 30887257 30887258 G A 26 GENIC homozygous 958868191 11 30889480 30889481 A G 29 GENIC homozygous 958868192 11 30889600 30889601 C T 24 GENIC homozygous 958868193 11 30889986 30889987 A G 15 GENIC homozygous 958868194 11 30892838 30892839 T C 14 GENIC homozygous 958868195