chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 50456263 50456264 A 19 GENIC homozygous 135906456 2 50456865 50456866 G C 25 GENIC homozygous 136104248 2 50458087 50458088 C G 28 GENIC homozygous 136104249 2 50458408 50458409 A G 20 GENIC homozygous 136104250 2 50458501 50458502 C G 22 GENIC homozygous 136104251 2 50458571 50458572 T C 24 GENIC homozygous 136104252 2 50459221 50459222 C T 19 GENIC homozygous 136104253 2 50460742 50460743 C T 17 GENIC homozygous 136104254 2 50461185 50461186 T C 18 GENIC homozygous 136104255 2 50461629 50461630 G T 27 GENIC homozygous 136104256 2 50462114 50462119 ATGAT 39 GENIC homozygous 135906457 2 50462962 50462963 C T 15 GENIC homozygous 136104257