chr start stop reference nuc variant nuc depth genic status zygosity variant ID 4 208845925 208845926 G GT 7 GENIC homozygous 57067241 4 208846156 208846157 G GGTGTGT 6 GENIC homozygous 57067242 4 208848127 208848128 T C 21 GENIC homozygous 57067245 4 208848897 208848898 A ATGTTT 17 GENIC homozygous 57067246 4 208848902 208848903 A T 19 GENIC homozygous 57067247 4 208849302 208849303 G A 30 GENIC homozygous 57067248 4 208850160 208850161 C CATT 18 GENIC homozygous 57067249 4 208850254 208850255 A AC 3 GENIC heterozygous 57067250 4 208850346 208850347 G T 12 GENIC homozygous 57067251 4 208850504 208850505 T C 16 GENIC homozygous 57067252 4 208850622 208850623 A G 19 GENIC homozygous 57067253 4 208850677 208850678 G GAC 21 GENIC homozygous 57067254 4 208851020 208851021 A C 9 GENIC homozygous 57067255 4 208851230 208851236 TGTGTA ------ 8 GENIC possibly homozygous 57067256 4 208851337 208851338 C T 16 GENIC homozygous 57067258 4 208851338 208851339 C G 15 GENIC homozygous 57067259 4 208851391 208851392 G GAC 15 GENIC homozygous 57067260 4 208851636 208851637 A - 10 GENIC homozygous 57067261 4 208851850 208851851 T C 26 GENIC homozygous 57067262 4 208851899 208851900 C T 26 GENIC homozygous 57067263 4 208852108 208852109 A G 41 GENIC homozygous 57067264 4 208852330 208852331 C G 26 GENIC homozygous 57067265