chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 69469688 69469689 A G 13 GENIC homozygous 791677275 17 69469716 69469717 G T 12 GENIC homozygous 791677276 17 69474447 69474448 T C 14 GENIC homozygous 791677277 17 69476128 69476129 T C 18 GENIC possibly homozygous 791677278 17 69477928 69477929 C T 13 GENIC homozygous 791677279 17 69478139 69478140 A G 9 GENIC homozygous 791677280 17 69478155 69478156 A G 10 GENIC homozygous 791677281 17 69478399 69478400 T C 21 GENIC homozygous 791677282 17 69479471 69479472 C A 2 GENIC homozygous 791677283 17 69479505 69479506 C T 3 GENIC homozygous 791677284 17 69479820 69479821 C A 22 GENIC heterozygous 791677285 17 69479821 69479822 C A 21 GENIC heterozygous 791677286 17 69479842 69479843 A C 24 GENIC heterozygous 791677287 17 69479958 69479959 A G 20 GENIC heterozygous 791677288 17 69479968 69479969 T C 12 GENIC heterozygous 791677289 17 69480197 69480198 A G 5 GENIC heterozygous 791677290 17 69483776 69483777 A G 42 GENIC heterozygous 791677291 17 69488124 69488125 A C 11 GENIC homozygous 791677292 17 69488653 69488654 T G 14 GENIC homozygous 791677293 17 69488844 69488845 C A 15 GENIC homozygous 791677294 17 69488848 69488849 A T 14 GENIC homozygous 791677295 17 69489677 69489678 A G 6 GENIC homozygous 791677296 17 69489701 69489702 G T 9 GENIC homozygous 791677297 17 69491352 69491353 A G 12 GENIC homozygous 791677298 17 69492952 69492953 G T 23 GENIC heterozygous 791677299 17 69493016 69493017 T A 16 GENIC possibly homozygous 791677300 17 69493017 69493018 C A 16 GENIC possibly homozygous 791677301 17 69493115 69493116 G A 14 GENIC possibly homozygous 791677302 17 69493689 69493690 G A 6 GENIC homozygous 791677303 17 69493968 69493969 C T 10 GENIC possibly homozygous 791677304 17 69493969 69493970 C T 11 GENIC possibly homozygous 791677305 17 69495591 69495592 C T 13 GENIC homozygous 791677306