chr start stop reference nuc variant nuc depth genic status zygosity variant ID 1 204838336 204838337 C T 49 GENIC homozygous 74678283 1 204838892 204838893 A G 45 GENIC homozygous 74678285 1 204840447 204840448 G A 53 GENIC possibly homozygous 74678287 1 204842984 204842985 G A 43 GENIC homozygous 74678289 1 204843595 204843596 T C 49 GENIC homozygous 74678291 1 204845150 204845151 T C 39 GENIC homozygous 74678293 1 204845891 204845892 A G 52 GENIC homozygous 74678295 1 204846036 204846037 T G 49 GENIC homozygous 74678297 1 204846351 204846352 G A 53 GENIC homozygous 74678299 1 204846745 204846746 G A 68 GENIC homozygous 74678301 1 204848500 204848501 T C 45 GENIC homozygous 74678303 1 204849122 204849123 C G 30 GENIC homozygous 74678305 1 204849200 204849201 G A 44 GENIC possibly homozygous 74678307 1 204852431 204852432 G A 36 GENIC homozygous 74678309 1 204852525 204852526 G T 49 GENIC homozygous 74678311 1 204853424 204853425 T C 45 GENIC possibly homozygous 74678313 1 204853572 204853573 T C 49 GENIC homozygous 74678315