chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 9937071 9937072 A G 22 GENIC homozygous 954698137 4 9937075 9937076 T C 21 GENIC homozygous 954698138 4 9937274 9937275 G A 31 GENIC homozygous 954698139 4 9937286 9937287 C T 33 GENIC homozygous 954698140 4 9937298 9937299 G A 33 GENIC homozygous 954698141 4 9937321 9937322 G A 38 GENIC homozygous 954698142 4 9937399 9937400 G A 31 GENIC homozygous 954698143 4 9937460 9937461 C A 34 GENIC homozygous 954698144 4 9937548 9937549 C T 24 GENIC homozygous 954698145 4 9937654 9937655 T G 20 GENIC homozygous 954698146 4 9937701 9937702 G A 16 GENIC homozygous 954698147 4 9937721 9937722 G A 17 GENIC homozygous 954698148 4 9937734 9937735 A C 17 GENIC homozygous 954698149 4 9937746 9937747 A G 15 GENIC homozygous 954698150 4 9937958 9937959 G T 29 GENIC homozygous 954698151 4 9938047 9938048 C G 33 GENIC homozygous 954698152 4 9938175 9938176 A G 32 GENIC homozygous 954698153 4 9938217 9938218 T A 24 GENIC homozygous 954698154 4 9938251 9938252 T A 25 GENIC homozygous 954698155 4 9938416 9938417 C G 21 GENIC homozygous 954698156 4 9938434 9938435 G T 20 GENIC homozygous 954698157 4 9938450 9938451 T C 19 GENIC homozygous 954698158 4 9938482 9938483 G T 19 GENIC homozygous 954698159 4 9938800 9938801 G T 21 GENIC homozygous 954698160 4 9938849 9938850 C T 31 GENIC homozygous 954698161 4 9938879 9938880 A G 34 GENIC homozygous 954698162 4 9938887 9938888 G C 38 GENIC homozygous 954698163