chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 11476782 11476783 C T 75 GENIC heterozygous 504793697 2 11476819 11476820 G T 78 GENIC heterozygous 504793698 2 11476832 11476833 A T 72 GENIC heterozygous 504793699 2 11476858 11476859 A T 59 GENIC heterozygous 504793700 2 11479365 11479366 T TATCTTA 12 GENIC homozygous 683484489 2 11484962 11484967 CGGGG ----- 17 GENIC heterozygous 683484490 2 11484962 11484965 CGG --- 17 GENIC heterozygous 683484491 2 11491538 11491539 G T 31 GENIC heterozygous 504793701 2 11516808 11516809 G A 88 GENIC heterozygous 504793702 2 11516861 11516862 C A 86 GENIC heterozygous 504793703 2 11516872 11516873 G A 80 GENIC heterozygous 504793704 2 11516876 11516877 A G 80 GENIC heterozygous 503047391 2 11516898 11516899 A G 85 GENIC heterozygous 504793705 2 11516994 11516995 A T 59 GENIC heterozygous 504793706 2 11517351 11517352 T G 16 GENIC heterozygous 504793707 2 11517395 11517396 C T 26 GENIC heterozygous 504793708 2 11517417 11517418 C T 28 GENIC heterozygous 504793709 2 11517418 11517419 G A 27 GENIC heterozygous 504793710 2 11517490 11517491 A G 22 GENIC heterozygous 504793711 2 11517614 11517615 A G 32 GENIC heterozygous 504793712 2 11517764 11517765 A G 34 GENIC possibly homozygous 504793713 2 11517776 11517777 C T 32 GENIC heterozygous 504793714 2 11517843 11517844 A G 32 GENIC heterozygous 504793715