chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 94238734 94238735 T C 21 GENIC homozygous 955698646 9 94238781 94238782 T C 25 GENIC homozygous 955698647 9 94238917 94238918 G A 25 GENIC homozygous 955698648 9 94238963 94238964 A G 33 GENIC homozygous 955698649 9 94239001 94239002 C T 37 GENIC homozygous 955698650 9 94239134 94239135 G A 49 GENIC homozygous 955698651 9 94239188 94239189 T C 42 GENIC homozygous 955698652 9 94239326 94239327 G A 34 GENIC homozygous 955698653 9 94240989 94240990 C T 25 GENIC homozygous 955698654 9 94242072 94242073 G C 24 GENIC homozygous 955698655 9 94242332 94242333 A G 33 GENIC homozygous 955698656 9 94242364 94242365 A C 29 GENIC homozygous 955698657 9 94247507 94247508 G A 23 GENIC homozygous 955698658 9 94247630 94247631 A C 28 GENIC homozygous 955698659 9 94247969 94247970 A G 40 GENIC homozygous 955698660 9 94248057 94248058 A T 29 GENIC homozygous 955698661 9 94248484 94248485 C G 28 GENIC homozygous 955698662 9 94249423 94249424 T C 27 GENIC homozygous 955698663 9 94250831 94250832 C T 26 GENIC possibly homozygous 955698664 9 94252124 94252125 A G 31 GENIC homozygous 955698665