chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 94238734 94238735 T C 29 GENIC homozygous 813041649 9 94238781 94238782 T C 27 GENIC homozygous 813041650 9 94238917 94238918 G A 28 GENIC homozygous 813041651 9 94238963 94238964 A G 25 GENIC homozygous 813041652 9 94239001 94239002 C T 31 GENIC homozygous 813041653 9 94239134 94239135 G A 35 GENIC homozygous 813041654 9 94239188 94239189 T C 31 GENIC homozygous 813041655 9 94239326 94239327 G A 30 GENIC homozygous 813041656 9 94240989 94240990 C T 13 GENIC possibly homozygous 813041657 9 94242072 94242073 G C 31 GENIC possibly homozygous 813041658 9 94242332 94242333 A G 27 GENIC homozygous 813041659 9 94242364 94242365 A C 30 GENIC homozygous 813041660 9 94244297 94244298 G C 43 GENIC homozygous 813041661 9 94247507 94247508 G A 51 GENIC homozygous 813041662 9 94247630 94247631 A C 21 GENIC homozygous 813041663 9 94247969 94247970 A G 27 GENIC homozygous 813041664 9 94248057 94248058 A T 26 GENIC homozygous 813041665 9 94248484 94248485 C G 38 GENIC homozygous 813041666 9 94249423 94249424 T C 27 GENIC homozygous 813041667 9 94250831 94250832 C T 29 GENIC homozygous 813041668 9 94252124 94252125 A G 34 INTERGENIC homozygous 813041669