chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 94238734 94238735 T C 17 GENIC homozygous 976454479 9 94238781 94238782 T C 14 GENIC homozygous 976454480 9 94238917 94238918 G A 32 GENIC homozygous 976454481 9 94238963 94238964 A G 40 GENIC homozygous 976454482 9 94239001 94239002 C T 35 GENIC homozygous 976454483 9 94239188 94239189 T C 18 GENIC homozygous 976454484 9 94239326 94239327 G A 23 GENIC homozygous 976454485 9 94240989 94240990 C T 29 GENIC homozygous 976454486 9 94242332 94242333 A G 23 GENIC homozygous 976454487 9 94242364 94242365 A C 24 GENIC homozygous 976454488 9 94244297 94244298 G C 12 GENIC homozygous 976454489 9 94245634 94245635 G A 12 GENIC homozygous 976454490 9 94246622 94246623 G A 14 GENIC homozygous 976454491 9 94247630 94247631 A C 9 GENIC homozygous 976454492 9 94247969 94247970 A G 6 GENIC homozygous 976454493 9 94248493 94248494 C T 8 GENIC homozygous 976454494 9 94249423 94249424 T C 17 GENIC homozygous 976454495 9 94250831 94250832 C T 6 GENIC homozygous 976454496 9 94252124 94252125 A G 9 GENIC homozygous 976454497