chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 94238734 94238735 T C 28 GENIC homozygous 944554597 9 94238781 94238782 T C 30 GENIC homozygous 944554598 9 94238917 94238918 G A 30 GENIC homozygous 944554599 9 94238963 94238964 A G 29 GENIC homozygous 944554600 9 94239001 94239002 C T 27 GENIC homozygous 944554601 9 94239134 94239135 G A 18 GENIC homozygous 944554602 9 94239188 94239189 T C 27 GENIC homozygous 944554603 9 94239326 94239327 G A 25 GENIC homozygous 944554604 9 94242072 94242073 G C 38 GENIC homozygous 944554605 9 94242332 94242333 A G 33 GENIC homozygous 944554606 9 94242364 94242365 A C 24 GENIC homozygous 944554607 9 94244297 94244298 G C 28 GENIC homozygous 944554608 9 94247507 94247508 G A 25 GENIC homozygous 944554609 9 94247630 94247631 A C 29 GENIC homozygous 944554610 9 94247969 94247970 A G 31 GENIC homozygous 944554611 9 94248057 94248058 A T 32 GENIC homozygous 944554612 9 94248484 94248485 C G 17 GENIC homozygous 944554613 9 94249423 94249424 T C 28 GENIC homozygous 944554614 9 94250831 94250832 C T 26 GENIC homozygous 944554615 9 94252124 94252125 A G 25 GENIC homozygous 944554616