chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 92269075 92269076 G T 2 GENIC homozygous 624987267 5 92269612 92269613 C CG 13 GENIC homozygous 740676871 5 92269820 92269821 C T 11 GENIC homozygous 624987268 5 92270228 92270229 G A 9 GENIC possibly homozygous 624987269 5 92270723 92270724 T C 3 GENIC homozygous 624987270 5 92271050 92271051 A G 4 GENIC homozygous 624987271 5 92271089 92271090 G A 5 GENIC homozygous 624987272 5 92272505 92272506 C T 18 GENIC possibly homozygous 624987273 5 92272790 92272791 G T 20 GENIC possibly homozygous 624987274 5 92272838 92272839 G T 9 GENIC possibly homozygous 624987275 5 92272913 92272914 A G 14 GENIC homozygous 624987276 5 92273832 92273833 T C 12 GENIC homozygous 624987277 5 92274188 92274189 C T 12 GENIC heterozygous 624987278 5 92274598 92274599 G A 2 GENIC heterozygous 624987279 5 92274645 92274646 A C 4 GENIC homozygous 624987280 5 92274922 92274923 A G 11 GENIC possibly homozygous 624987281 5 92275069 92275070 G A 11 GENIC homozygous 624987282 5 92275714 92275715 T G 8 GENIC homozygous 624987283 5 92276027 92276028 G A 14 GENIC possibly homozygous 624987284 5 92276604 92276605 C G 8 GENIC heterozygous 624987285