chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 94238734 94238735 T C 27 GENIC homozygous 803919503 9 94238781 94238782 T C 44 GENIC homozygous 803919504 9 94238917 94238918 G A 30 GENIC homozygous 803919505 9 94238963 94238964 A G 20 GENIC homozygous 803919506 9 94239001 94239002 C T 26 GENIC homozygous 803919507 9 94239134 94239135 G A 34 GENIC homozygous 803919508 9 94239188 94239189 T C 35 GENIC homozygous 803919509 9 94239326 94239327 G A 30 GENIC homozygous 803919510 9 94240989 94240990 C T 29 GENIC possibly homozygous 803919511 9 94242072 94242073 G C 32 GENIC homozygous 803919512 9 94242332 94242333 A G 27 GENIC homozygous 803919513 9 94242364 94242365 A C 30 GENIC homozygous 803919514 9 94244297 94244298 G C 23 GENIC homozygous 803919515 9 94247507 94247508 G A 26 GENIC homozygous 803919516 9 94247630 94247631 A C 37 GENIC homozygous 803919517 9 94247969 94247970 A G 31 GENIC homozygous 803919518 9 94248057 94248058 A T 21 GENIC homozygous 803919519 9 94248484 94248485 C G 41 GENIC homozygous 803919520 9 94249423 94249424 T C 20 GENIC homozygous 803919521 9 94250831 94250832 C T 36 GENIC homozygous 803919522 9 94252124 94252125 A G 39 INTERGENIC homozygous 803919523