chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 175446141 175446142 T G 28 GENIC homozygous 112961305 4 175446150 175446151 T G 27 GENIC homozygous 112961307 4 175446152 175446153 C G 28 GENIC homozygous 112961309 4 175446155 175446156 T G 28 GENIC homozygous 112961311 4 175446158 175446159 T G 28 GENIC homozygous 112961313 4 175446164 175446165 A G 29 GENIC homozygous 112961315 4 175446175 175446176 G T 28 GENIC homozygous 112961317 4 175446176 175446177 C T 28 GENIC homozygous 112961319 4 175452838 175452839 A G 16 GENIC homozygous 113222261 4 175500432 175500433 T G 37 GENIC homozygous 112961438 4 175506052 175506053 T C 23 GENIC homozygous 112961446 4 175652665 175652666 G T 28 GENIC homozygous 112961627 4 175658760 175658761 T A 21 GENIC heterozygous 119458821 4 175658761 175658762 G A 20 GENIC heterozygous 119458822 4 175658791 175658792 C T 26 GENIC heterozygous 119457686 4 175658792 175658793 G C 26 GENIC heterozygous 119457687 4 175658795 175658796 T C 27 GENIC heterozygous 113068364 4 175658949 175658950 A C 28 GENIC heterozygous 119467104 4 175658951 175658952 T C 26 GENIC heterozygous 112961645 4 175658970 175658971 C T 27 GENIC heterozygous 112961647