chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 14308797 14308798 G GTT 1 GENIC homozygous 51623018 10 14309216 14309217 T G 17 GENIC heterozygous 51623019 10 14310299 14310300 G A 15 GENIC possibly homozygous 51623020 10 14311196 14311197 A G 10 GENIC heterozygous 51623021 10 14311238 14311239 C T 17 GENIC possibly homozygous 51623022 10 14312934 14312935 G A 11 GENIC homozygous 51623024 10 14313184 14313185 A AGTGTGT 3 GENIC heterozygous 51623025 10 14313414 14313415 T TG 12 GENIC homozygous 51329162 10 14313935 14313936 A C 24 GENIC possibly homozygous 51623026 10 14315089 14315203 GGATTGTGGGGTCCAGCACCTGTGCTCCACTATAGCCAGGATTGTGGGGTCCAGCACCTGTGCTCCACTATAGCCAGGATTGTGGGGTCCAGCACCTGTGCTCCACTGTAGCCC ------------------------------------------------------------------------------------------------------------------ 14 GENIC possibly homozygous 52313057 10 14316323 14316324 T C 16 GENIC possibly homozygous 51623038 10 14316457 14316458 G - 21 GENIC possibly homozygous 51623039 10 14317185 14317186 A G 21 GENIC homozygous 51623040 10 14318870 14318871 G C 13 GENIC homozygous 51623044 10 14320293 14320294 C A 24 GENIC possibly homozygous 51623045 10 14321209 14321210 T G 8 GENIC homozygous 51623046 10 14324591 14324592 A G 13 GENIC homozygous 51623047 10 14325784 14325785 T A 29 GENIC homozygous 51623048 10 14331372 14331373 G T 17 GENIC homozygous 51623049 10 14331520 14331521 T A 23 GENIC homozygous 51623050