chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 107470604 107470604 A 21 GENIC possibly homozygous 145648059 8 107475268 107475269 T 25 GENIC possibly homozygous 138263310 8 107478418 107478418 C 23 GENIC homozygous 138263311 8 107478533 107478534 A T 28 GENIC homozygous 138410153 8 107480940 107480941 T C 16 GENIC homozygous 145674171 8 107482237 107482241 ACAT 9 GENIC heterozygous 145648060 8 107486675 107486676 G A 24 GENIC homozygous 138410155 8 107492200 107492201 G A 30 GENIC homozygous 145674172 8 107492359 107492360 C T 21 GENIC homozygous 142099346 8 107496368 107496368 ATT 13 GENIC homozygous 145648061 8 107507302 107507303 G A 21 GENIC homozygous 145674173 8 107494376 107494377 T G 23 GENIC homozygous 138410157 8 107496877 107496878 T C 29 GENIC homozygous 138410158 8 107505897 107505898 T C 21 GENIC homozygous 138410159 8 107507063 107507064 G T 17 GENIC homozygous 138410160 8 107509478 107509479 T C 30 GENIC homozygous 138410161 8 107509587 107509588 T C 19 GENIC homozygous 138410162 8 107510365 107510366 C T 25 GENIC homozygous 145674174 8 107512910 107512911 T C 13 GENIC homozygous 138410163 8 107520619 107520620 G A 17 GENIC homozygous 138410164 8 107523440 107523441 G T 29 GENIC homozygous 138410165 8 107526497 107526498 T C 25 GENIC homozygous 138410167 8 107527791 107527792 T A 32 GENIC homozygous 138410169 8 107531327 107531328 C T 38 GENIC homozygous 138410170 8 107532663 107532664 T C 23 GENIC homozygous 142099388 8 107534901 107534902 T 37 GENIC homozygous 138263315 8 107535553 107535554 G T 29 GENIC homozygous 138410171 8 107535668 107535669 A C 23 GENIC homozygous 145674175 8 107536012 107536013 G A 25 GENIC homozygous 138410172 8 107538820 107538820 GACAAG 26 GENIC homozygous 138263316 8 107540593 107540593 A 31 GENIC possibly homozygous 138263317