chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 205016984 205016985 G A 29 GENIC possibly homozygous 120511636 1 205021256 205021257 G T 23 GENIC homozygous 120511637 1 205021765 205021766 G T 31 GENIC homozygous 120511638 1 205022813 205022814 A G 14 GENIC homozygous 120733161 1 205023058 205023059 C T 25 GENIC homozygous 120511639 1 205023071 205023072 G A 27 GENIC homozygous 120511640 1 205024933 205024934 T C 22 GENIC homozygous 120511641 1 205025159 205025160 G A 23 GENIC heterozygous 120733163 1 205025699 205025700 C T 35 GENIC possibly homozygous 120511642 1 205025710 205025711 A G 35 GENIC homozygous 120511643 1 205025995 205025996 C T 29 GENIC homozygous 120511644 1 205026145 205026146 C T 27 GENIC homozygous 120511645 1 205026146 205026147 G C 27 GENIC homozygous 120511646 1 205026220 205026221 G A 20 GENIC homozygous 120511647 1 205026228 205026229 C T 19 GENIC homozygous 120511648 1 205026349 205026350 T C 17 GENIC homozygous 120511649 1 205026497 205026498 C A 18 GENIC homozygous 120511650 1 205027080 205027081 C T 15 GENIC homozygous 120511652 1 205027562 205027563 G A 24 GENIC homozygous 120511653 1 205027851 205027852 C A 29 GENIC homozygous 120511654 1 205027869 205027870 C T 23 GENIC homozygous 120511655 1 205028814 205028815 A G 19 GENIC homozygous 120511656