chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 94238734 94238735 T C 29 GENIC homozygous 883840452 9 94238781 94238782 T C 26 GENIC homozygous 883840453 9 94238917 94238918 G A 32 GENIC homozygous 883840454 9 94238963 94238964 A G 22 GENIC homozygous 883840455 9 94239001 94239002 C T 33 GENIC homozygous 883840456 9 94239134 94239135 G A 17 GENIC homozygous 883840457 9 94239188 94239189 T C 13 GENIC homozygous 883840458 9 94239326 94239327 G A 22 GENIC homozygous 883840459 9 94242072 94242073 G C 20 GENIC homozygous 883840460 9 94242332 94242333 A G 27 GENIC homozygous 883840461 9 94242364 94242365 A C 26 GENIC homozygous 883840462 9 94247507 94247508 G A 38 GENIC homozygous 883840463 9 94247630 94247631 A C 20 GENIC homozygous 883840464 9 94247969 94247970 A G 13 GENIC homozygous 883840465 9 94248057 94248058 A T 21 GENIC homozygous 883840466 9 94248484 94248485 C G 23 GENIC homozygous 883840467 9 94249423 94249424 T C 20 GENIC homozygous 883840468 9 94250831 94250832 C T 25 GENIC homozygous 883840469