chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 94238734 94238735 T C 25 GENIC homozygous 964571393 9 94238781 94238782 T C 23 GENIC homozygous 964571394 9 94238917 94238918 G A 27 GENIC homozygous 964571395 9 94238963 94238964 A G 29 GENIC homozygous 964571396 9 94239001 94239002 C T 28 GENIC homozygous 964571397 9 94239134 94239135 G A 38 GENIC homozygous 964571398 9 94239188 94239189 T C 38 GENIC homozygous 964571399 9 94239326 94239327 G A 34 GENIC homozygous 964571400 9 94240989 94240990 C T 13 GENIC homozygous 964571401 9 94242072 94242073 G C 24 GENIC homozygous 964571402 9 94242332 94242333 A G 29 GENIC homozygous 964571403 9 94242364 94242365 A C 26 GENIC homozygous 964571404 9 94244297 94244298 G C 41 GENIC homozygous 964571405 9 94247507 94247508 G A 26 GENIC homozygous 964571406 9 94247630 94247631 A C 21 GENIC homozygous 964571407 9 94247969 94247970 A G 31 GENIC homozygous 964571408 9 94248057 94248058 A T 26 GENIC homozygous 964571409 9 94248484 94248485 C G 26 GENIC homozygous 964571410 9 94249423 94249424 T C 32 GENIC homozygous 964571411 9 94250831 94250832 C T 19 GENIC homozygous 964571412 9 94252124 94252125 A G 23 GENIC possibly homozygous 964571413