chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 94487529 94487530 C T 18 GENIC heterozygous 52280663 9 94488368 94488369 G T 8 GENIC heterozygous 52280664 9 94489668 94489669 C T 11 GENIC homozygous 52280665 9 94490270 94490271 A AG 18 GENIC possibly homozygous 52280666 9 94490375 94490376 T C 20 GENIC possibly homozygous 52280667 9 94491050 94491051 A G 15 GENIC possibly homozygous 52053579 9 94491382 94491383 T C 11 GENIC possibly homozygous 52053583 9 94492018 94492019 T A 15 GENIC possibly homozygous 52280673 9 94492047 94492048 G A 18 GENIC homozygous 52280674 9 94492281 94492282 C A 14 GENIC homozygous 52053589 9 94492466 94492467 C T 22 GENIC possibly homozygous 52280675 9 94492497 94492498 G GCA 4 GENIC heterozygous 52053593 9 94492893 94492894 G - 5 GENIC heterozygous 52280676 9 94493500 94493506 ACACAC ------ 5 GENIC heterozygous 52280678 9 94493522 94493523 A G 8 GENIC homozygous 52280680 9 94494024 94494025 G C 16 GENIC homozygous 52280681 9 94494774 94494775 C G 12 GENIC heterozygous 52280683