chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 91206966 91206967 C T 12 GENIC homozygous 876431135 3 91207854 91207855 A G 10 GENIC homozygous 876431136 3 91207888 91207889 T G 16 GENIC homozygous 876431137 3 91208211 91208212 G A 12 GENIC homozygous 876431138 3 91208274 91208275 T C 18 GENIC homozygous 876431139 3 91208366 91208367 T C 16 GENIC homozygous 876431140 3 91208938 91208939 G A 12 GENIC homozygous 876431141 3 91208961 91208962 A G 15 GENIC homozygous 876431142 3 91209026 91209027 A C 16 GENIC homozygous 876431143 3 91209172 91209173 A G 14 GENIC homozygous 876431144 3 91209557 91209558 A G 29 GENIC homozygous 876431145 3 91209950 91209951 C T 33 GENIC homozygous 876431146 3 91210148 91210149 C T 22 GENIC homozygous 876431147 3 91210943 91210944 T G 22 GENIC homozygous 876431148 3 91211310 91211311 A G 25 GENIC homozygous 876431149 3 91211824 91211825 G C 14 GENIC homozygous 876431150 3 91213023 91213024 C A 6 GENIC homozygous 876431151 3 91213078 91213079 T C 13 GENIC homozygous 876431152 3 91213347 91213348 A G 9 GENIC homozygous 876431153 3 91213418 91213419 C T 11 GENIC homozygous 876431154 3 91215339 91215340 G A 7 GENIC homozygous 876431155