chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 103300578 103300579 C T 28 GENIC homozygous 109420284 1 103305648 103305649 C T 18 GENIC homozygous 109116668 1 103307196 103307197 A G 17 GENIC homozygous 109116686 1 103308678 103308679 G A 13 GENIC homozygous 109420290 1 103308758 103308759 A C 21 GENIC homozygous 109116700 1 103308937 103308938 C T 27 GENIC homozygous 109420292 1 103309191 103309192 C T 14 GENIC homozygous 109420294 1 103309901 103309902 C T 17 GENIC homozygous 109420296 1 103311085 103311086 G A 15 GENIC possibly homozygous 109420298 1 103311109 103311110 C T 15 GENIC homozygous 109116708 1 103311176 103311177 G T 15 GENIC homozygous 109420300 1 103311719 103311720 A T 18 GENIC homozygous 108165384 1 103311942 103311943 A G 26 GENIC homozygous 109116718 1 103312358 103312359 G A 23 GENIC homozygous 109420302 1 103313126 103313127 G A 20 GENIC homozygous 109420304 1 103313600 103313601 G A 18 GENIC homozygous 109116734 1 103313813 103313814 C T 18 GENIC homozygous 109116739 1 103313993 103313994 C T 26 GENIC homozygous 109420306 1 103315867 103315868 T G 12 GENIC homozygous 109116757 1 103316063 103316064 G A 9 GENIC homozygous 109420308 1 103320973 103320974 T C 18 GENIC homozygous 109116770 1 103321069 103321070 A G 15 GENIC homozygous 109116772 1 103321105 103321106 G A 15 GENIC homozygous 109420315 1 103321455 103321456 C T 23 GENIC homozygous 108903064 1 103321464 103321465 G A 23 GENIC homozygous 109116774 1 103321665 103321666 C T 18 GENIC homozygous 108903065 1 103321752 103321753 G A 14 GENIC homozygous 109116776 1 103322494 103322495 A G 8 GENIC homozygous 108903066 1 103322525 103322526 A G 8 GENIC homozygous 108903067 1 103322937 103322938 G A 17 GENIC homozygous 109420317 1 103323300 103323301 A C 28 GENIC homozygous 109116778