chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 59490763 59490764 A G 20 GENIC homozygous 960937242 5 59491034 59491035 G A 24 GENIC homozygous 960937243 5 59492252 59492253 G A 26 GENIC homozygous 960937244 5 59493293 59493294 T C 30 GENIC homozygous 960937245 5 59493344 59493345 C T 24 GENIC possibly homozygous 960937246 5 59494021 59494022 G T 21 GENIC homozygous 960937247 5 59495021 59495022 A G 29 GENIC homozygous 960937248 5 59496242 59496243 A G 24 GENIC homozygous 960937249 5 59497270 59497271 G A 23 GENIC homozygous 960937250 5 59500179 59500180 A G 28 GENIC homozygous 960937251 5 59500828 59500829 G C 35 GENIC homozygous 960937252 5 59500873 59500874 G A 38 GENIC homozygous 960937253 5 59500875 59500876 C T 39 GENIC homozygous 960937254 5 59502207 59502208 C A 30 GENIC homozygous 960937255 5 59502243 59502244 C T 31 GENIC homozygous 960937256 5 59502300 59502301 G A 26 GENIC homozygous 960937257 5 59502340 59502341 C T 20 GENIC homozygous 960937258 5 59502468 59502469 C T 27 GENIC homozygous 960937259 5 59502683 59502684 T C 17 GENIC homozygous 960937260 5 59502698 59502699 A T 17 GENIC homozygous 960937261 5 59502746 59502747 A G 13 GENIC homozygous 960937262 5 59503232 59503233 C T 15 GENIC homozygous 960937263 5 59503453 59503454 C T 28 GENIC homozygous 960937264 5 59503514 59503515 T C 26 GENIC homozygous 960937265 5 59503720 59503721 T C 23 GENIC homozygous 960937266 5 59504116 59504117 T C 14 GENIC homozygous 960937267 5 59504488 59504489 A G 24 GENIC homozygous 960937268 5 59504888 59504889 T C 12 GENIC homozygous 960937269 5 59505140 59505141 C T 31 GENIC homozygous 960937270 5 59505463 59505464 T C 29 GENIC homozygous 960937271 5 59505718 59505719 G A 20 GENIC homozygous 960937272