chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 94238734 94238735 T C 8 GENIC homozygous 950462142 9 94238781 94238782 T C 11 GENIC homozygous 950462143 9 94238917 94238918 G A 18 GENIC homozygous 950462144 9 94238963 94238964 A G 9 GENIC homozygous 950462145 9 94239001 94239002 C T 7 GENIC homozygous 950462146 9 94239134 94239135 G A 11 GENIC homozygous 950462147 9 94239188 94239189 T C 12 GENIC homozygous 950462148 9 94239326 94239327 G A 13 GENIC homozygous 950462149 9 94240989 94240990 C T 21 GENIC homozygous 950462150 9 94242072 94242073 G C 8 GENIC homozygous 950462151 9 94242332 94242333 A G 11 GENIC homozygous 950462152 9 94242364 94242365 A C 13 GENIC homozygous 950462153 9 94244297 94244298 G C 14 GENIC homozygous 950462154 9 94247507 94247508 G A 15 GENIC homozygous 950462155 9 94247630 94247631 A C 12 GENIC homozygous 950462156 9 94247969 94247970 A G 7 GENIC homozygous 950462157 9 94248057 94248058 A T 10 GENIC homozygous 950462158 9 94248484 94248485 C G 8 GENIC homozygous 950462159 9 94249423 94249424 T C 18 GENIC homozygous 950462160 9 94250831 94250832 C T 8 GENIC homozygous 950462161 9 94252124 94252125 A G 7 GENIC homozygous 950462162