chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 91206699 91206700 A T 8 GENIC homozygous 879606141 3 91206710 91206711 T A 11 GENIC homozygous 879606142 3 91206966 91206967 C T 13 GENIC homozygous 879606143 3 91207888 91207889 T G 15 GENIC homozygous 879606144 3 91208211 91208212 G A 10 GENIC homozygous 879606145 3 91208274 91208275 T C 21 GENIC homozygous 879606146 3 91208366 91208367 T C 16 GENIC homozygous 879606147 3 91208897 91208898 A G 5 GENIC heterozygous 879606148 3 91208898 91208899 G T 5 GENIC heterozygous 879606149 3 91208899 91208900 T A 6 GENIC homozygous 879606150 3 91208938 91208939 G A 16 GENIC homozygous 879606151 3 91208961 91208962 A G 20 GENIC homozygous 879606152 3 91209026 91209027 A C 13 GENIC homozygous 879606153 3 91209172 91209173 A G 17 GENIC homozygous 879606154 3 91209557 91209558 A G 20 GENIC homozygous 879606155 3 91209950 91209951 C T 18 GENIC homozygous 879606156 3 91210148 91210149 C T 16 GENIC homozygous 879606157 3 91210943 91210944 T G 16 GENIC homozygous 879606158 3 91211310 91211311 A G 19 GENIC homozygous 879606159 3 91213023 91213024 C A 11 GENIC homozygous 879606160 3 91213078 91213079 T C 14 GENIC homozygous 879606161 3 91213347 91213348 A G 15 GENIC homozygous 879606162 3 91213418 91213419 C T 17 GENIC homozygous 879606163 3 91215339 91215340 G A 21 GENIC homozygous 879606164