chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 69695928 69695929 A T 13 GENIC homozygous 787392292 17 69697819 69697820 G A 21 GENIC homozygous 787392293 17 69697984 69697985 C T 28 GENIC homozygous 787392294 17 69698704 69698705 T C 20 GENIC homozygous 787392295 17 69698857 69698858 A G 24 GENIC homozygous 787392296 17 69699396 69699397 G A 9 GENIC homozygous 787392297 17 69699404 69699405 T G 9 GENIC homozygous 787392298 17 69699503 69699504 A G 12 GENIC homozygous 787392299 17 69700994 69700995 C T 23 GENIC possibly homozygous 787392300 17 69701271 69701272 C T 20 GENIC homozygous 787392301 17 69701553 69701554 G A 36 GENIC homozygous 787392302 17 69702434 69702435 C A 33 GENIC possibly homozygous 787392303 17 69702943 69702944 T C 29 GENIC homozygous 787392304 17 69703338 69703339 G T 28 GENIC homozygous 787392305 17 69703537 69703538 G T 58 GENIC heterozygous 787392306 17 69703706 69703707 C T 89 GENIC heterozygous 787392307 17 69703717 69703718 C T 84 GENIC heterozygous 787392308 17 69704504 69704505 G A 38 GENIC homozygous 787392309 17 69709179 69709180 T C 33 GENIC homozygous 787392310 17 69711333 69711334 T G 17 GENIC homozygous 787392311