chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 94238734 94238735 T C 25 GENIC homozygous 938777010 9 94238781 94238782 T C 23 GENIC homozygous 938777011 9 94238917 94238918 G A 19 GENIC homozygous 938777012 9 94238963 94238964 A G 21 GENIC homozygous 938777013 9 94239001 94239002 C T 27 GENIC homozygous 938777014 9 94239134 94239135 G A 13 GENIC homozygous 938777015 9 94239188 94239189 T C 26 GENIC homozygous 938777016 9 94239326 94239327 G A 18 GENIC homozygous 938777017 9 94240989 94240990 C T 20 GENIC homozygous 938777018 9 94242072 94242073 G C 16 GENIC homozygous 938777019 9 94242332 94242333 A G 17 GENIC homozygous 938777020 9 94242364 94242365 A C 25 GENIC homozygous 938777021 9 94244297 94244298 G C 23 GENIC homozygous 938777022 9 94247507 94247508 G A 19 GENIC homozygous 938777023 9 94247630 94247631 A C 21 GENIC homozygous 938777024 9 94247969 94247970 A G 38 GENIC homozygous 938777025 9 94248057 94248058 A T 28 GENIC homozygous 938777026 9 94248484 94248485 C G 13 GENIC homozygous 938777027 9 94249423 94249424 T C 27 GENIC homozygous 938777028 9 94250831 94250832 C T 21 GENIC homozygous 938777029 9 94252124 94252125 A G 26 GENIC homozygous 938777030