chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 16016426 16016427 T C 26 GENIC homozygous 50076243 12 16016457 16016458 G A 31 GENIC homozygous 50668699 12 16017201 16017207 TGTGTG ------ 19 GENIC heterozygous 50502604 12 16017203 16017207 TGTG ---- 19 GENIC heterozygous 50822865 12 16019361 16019362 G A 15 GENIC homozygous 50668701 12 16020255 16020256 T C 23 GENIC homozygous 50076250 12 16020556 16020557 G A 29 GENIC homozygous 50668704 12 16020974 16020975 A T 24 GENIC homozygous 50076256 12 16021286 16021287 T G 14 GENIC homozygous 50076260 12 16021674 16021675 T A 17 GENIC homozygous 50668706 12 16023486 16023487 A T 11 GENIC homozygous 50076272 12 16023521 16023522 A G 14 GENIC homozygous 50502611 12 16024045 16024046 G A 20 GENIC homozygous 50668709 12 16025118 16025119 A G 17 GENIC homozygous 50076288 12 16025266 16025267 A G 9 GENIC homozygous 50076290 12 16025934 16025935 G A 9 INTERGENIC homozygous 50668711 12 16025986 16025987 C T 13 INTERGENIC homozygous 50668713 12 16026015 16026016 T C 17 INTERGENIC homozygous 50076294 12 16026054 16026055 A T 13 INTERGENIC homozygous 50668715 12 16023459 16023462 CTC --- 10 GENIC homozygous 50907638 12 16025812 16025813 T C 6 INTERGENIC homozygous 50923654 12 16026083 16026084 G C 8 INTERGENIC homozygous 50923657 12 16026084 16026085 G C 8 INTERGENIC homozygous 50923660 12 16026086 16026087 C CTGCCCTCCAACCTCTGCTGCTGGAATTAAATGTGCT 8 INTERGENIC homozygous 50923663 12 16026911 16026917 TTTTTT ------ 7 INTERGENIC heterozygous 50614153 12 16027029 16027030 T C 33 INTERGENIC homozygous 50668719 12 16027508 16027509 T C 25 INTERGENIC homozygous 50668721 12 16027760 16027761 C T 24 INTERGENIC homozygous 50668724 12 16028312 16028313 G A 21 INTERGENIC homozygous 50923666 12 16028363 16028364 A AT 15 INTERGENIC homozygous 50923669 12 16028369 16028370 C T 16 INTERGENIC homozygous 50076300 12 16028411 16028412 T - 17 INTERGENIC possibly homozygous 50822867