chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 94238734 94238735 T C 70 GENIC homozygous 808517405 9 94238781 94238782 T C 58 GENIC homozygous 808517406 9 94238917 94238918 G A 76 GENIC homozygous 808517407 9 94238963 94238964 A G 49 GENIC homozygous 808517408 9 94239001 94239002 C T 42 GENIC homozygous 808517409 9 94239134 94239135 G A 52 GENIC homozygous 808517410 9 94239188 94239189 T C 66 GENIC homozygous 808517411 9 94239326 94239327 G A 48 GENIC homozygous 808517412 9 94240989 94240990 C T 64 GENIC possibly homozygous 808517413 9 94242072 94242073 G C 32 GENIC homozygous 808517414 9 94242332 94242333 A G 50 GENIC homozygous 808517415 9 94242364 94242365 A C 48 GENIC possibly homozygous 808517416 9 94244297 94244298 G C 48 GENIC homozygous 808517417 9 94247507 94247508 G A 60 GENIC homozygous 808517418 9 94247630 94247631 A C 47 GENIC homozygous 808517419 9 94247969 94247970 A G 55 GENIC homozygous 808517420 9 94248057 94248058 A T 55 GENIC homozygous 808517421 9 94248484 94248485 C G 34 GENIC homozygous 808517422 9 94249423 94249424 T C 49 GENIC possibly homozygous 808517423 9 94250831 94250832 C T 44 GENIC homozygous 808517424 9 94252124 94252125 A G 47 INTERGENIC possibly homozygous 808517425