chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 94238734 94238735 T C 24 GENIC homozygous 973243195 9 94238781 94238782 T C 43 GENIC homozygous 973243196 9 94238917 94238918 G A 29 GENIC homozygous 973243197 9 94238963 94238964 A G 20 GENIC homozygous 973243198 9 94239001 94239002 C T 26 GENIC homozygous 973243199 9 94239134 94239135 G A 34 GENIC homozygous 973243200 9 94239188 94239189 T C 35 GENIC homozygous 973243201 9 94239326 94239327 G A 32 GENIC homozygous 973243202 9 94240989 94240990 C T 25 GENIC homozygous 973243203 9 94242072 94242073 G C 31 GENIC homozygous 973243204 9 94242332 94242333 A G 28 GENIC homozygous 973243205 9 94242364 94242365 A C 31 GENIC homozygous 973243206 9 94244297 94244298 G C 23 GENIC homozygous 973243207 9 94247507 94247508 G A 26 GENIC homozygous 973243208 9 94247630 94247631 A C 36 GENIC homozygous 973243209 9 94247969 94247970 A G 29 GENIC homozygous 973243210 9 94248057 94248058 A T 19 GENIC homozygous 973243211 9 94248484 94248485 C G 39 GENIC homozygous 973243212 9 94249423 94249424 T C 19 GENIC homozygous 973243213 9 94250831 94250832 C T 35 GENIC homozygous 973243214 9 94252124 94252125 A G 39 GENIC homozygous 973243215