chr start stop reference nuc variant nuc depth genic status zygosity variant ID 6 41020059 41020060 A C 50 GENIC homozygous 114768794 6 41020388 41020389 G A 62 GENIC homozygous 115205730 6 41020627 41020628 C G 54 GENIC homozygous 115205731 6 41021574 41021575 A C 61 GENIC homozygous 114768810 6 41021613 41021614 C A 63 GENIC homozygous 114768812 6 41021654 41021655 G A 67 GENIC homozygous 114768814 6 41022469 41022470 C A 49 GENIC homozygous 114768816 6 41023796 41023797 C T 75 GENIC homozygous 114768818 6 41023828 41023829 C T 75 GENIC homozygous 114768820 6 41023987 41023988 G A 68 GENIC homozygous 114768822 6 41024160 41024161 A T 56 GENIC homozygous 114768824 6 41024423 41024424 G T 61 GENIC homozygous 114768828 6 41024735 41024736 A G 55 GENIC homozygous 114768830 6 41026772 41026773 G T 73 GENIC homozygous 114768834 6 41027806 41027807 C G 53 GENIC homozygous 118647884 6 41033488 41033488 TC 70 GENIC homozygous 128331880 6 41036274 41036278 GACC 71 GENIC homozygous 128331882 6 41038361 41038365 AACC 62 GENIC homozygous 132092945 6 41025162 41025163 T A 53 GENIC homozygous 118553043 6 41025163 41025164 A T 53 GENIC homozygous 118553044 6 41026515 41026516 C T 72 GENIC homozygous 115374685 6 41027020 41027021 G A 64 GENIC homozygous 115374687 6 41030329 41030330 A G 55 GENIC homozygous 115374689 6 41028511 41028513 GC 37 GENIC homozygous 132092943 6 41034522 41034522 GG 59 GENIC homozygous 132092944 6 41038471 41038471 C 70 GENIC homozygous 128331885 6 41039339 41039339 T 46 GENIC possibly homozygous 131408010