chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 94238734 94238735 T C 53 GENIC homozygous 781322990 9 94238781 94238782 T C 42 GENIC homozygous 781322991 9 94238917 94238918 G A 55 GENIC homozygous 781322992 9 94238963 94238964 A G 49 GENIC homozygous 781322993 9 94239001 94239002 C T 54 GENIC homozygous 781322994 9 94239134 94239135 G A 46 GENIC homozygous 781322995 9 94239188 94239189 T C 37 GENIC homozygous 781322996 9 94239326 94239327 G A 47 GENIC homozygous 781322997 9 94240989 94240990 C T 101 GENIC possibly homozygous 781322998 9 94242072 94242073 G C 61 GENIC possibly homozygous 781322999 9 94242332 94242333 A G 72 GENIC possibly homozygous 781323000 9 94242364 94242365 A C 66 GENIC homozygous 781323001 9 94244297 94244298 G C 58 GENIC homozygous 781323002 9 94247507 94247508 G A 55 GENIC homozygous 781323003 9 94247630 94247631 A C 47 GENIC homozygous 781323004 9 94247969 94247970 A G 45 GENIC homozygous 781323005 9 94248057 94248058 A T 62 GENIC homozygous 781323006 9 94248484 94248485 C G 44 GENIC possibly homozygous 781323007 9 94249423 94249424 T C 74 GENIC homozygous 781323008 9 94250831 94250832 C T 54 GENIC homozygous 781323009 9 94252124 94252125 A G 69 INTERGENIC homozygous 781323010