chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 180897138 180897139 G A 23 GENIC heterozygous 993028454 2 180898138 180898139 A G 19 GENIC homozygous 993028455 2 180898172 180898173 G A 20 GENIC homozygous 993028456 2 180899056 180899057 C A 27 GENIC homozygous 993028457 2 180899134 180899135 G A 20 GENIC homozygous 993028458 2 180899312 180899313 A G 12 GENIC homozygous 993028459 2 180899631 180899632 T C 23 GENIC homozygous 993028460 2 180899755 180899756 C T 29 GENIC possibly homozygous 993028461 2 180901332 180901333 T C 18 GENIC homozygous 993028462 2 180902408 180902409 A G 18 GENIC homozygous 993028463 2 180903152 180903153 A T 22 GENIC possibly homozygous 993028464 2 180906629 180906630 A C 20 GENIC possibly homozygous 993028465 2 180907151 180907152 T C 20 GENIC homozygous 993028466 2 180907719 180907720 T A 17 GENIC homozygous 993028467 2 180908056 180908057 T A 21 GENIC homozygous 993028468 2 180908111 180908112 G A 19 GENIC homozygous 993028469 2 180910701 180910702 A C 15 GENIC homozygous 993028470 2 180911479 180911480 T C 29 GENIC homozygous 993028471 2 180911824 180911825 C G 30 GENIC homozygous 993028472 2 180911828 180911829 G A 32 GENIC homozygous 993028473