chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 94238734 94238735 T C 27 GENIC homozygous 952976886 9 94238781 94238782 T C 25 GENIC homozygous 952976887 9 94238917 94238918 G A 34 GENIC homozygous 952976888 9 94238963 94238964 A G 47 GENIC homozygous 952976889 9 94239001 94239002 C T 43 GENIC homozygous 952976890 9 94239134 94239135 G A 19 GENIC homozygous 952976891 9 94239188 94239189 T C 29 GENIC possibly homozygous 952976892 9 94239326 94239327 G A 28 GENIC homozygous 952976893 9 94240989 94240990 C T 24 GENIC homozygous 952976894 9 94242072 94242073 G C 12 GENIC homozygous 952976895 9 94242332 94242333 A G 14 GENIC homozygous 952976896 9 94242364 94242365 A C 19 GENIC homozygous 952976897 9 94247630 94247631 A C 21 GENIC homozygous 952976898 9 94247969 94247970 A G 24 GENIC homozygous 952976899 9 94248057 94248058 A T 17 GENIC homozygous 952976900 9 94248484 94248485 C G 14 GENIC homozygous 952976901 9 94249423 94249424 T C 21 GENIC homozygous 952976902 9 94250831 94250832 C T 20 GENIC homozygous 952976903 9 94252124 94252125 A G 26 GENIC homozygous 952976904