chr start stop reference nuc variant nuc depth genic status zygosity variant ID 3 120166209 120166210 C G 20 GENIC homozygous 957606238 3 120166244 120166245 T C 20 GENIC homozygous 957606239 3 120166256 120166257 G A 22 GENIC homozygous 957606240 3 120167883 120167884 T C 19 GENIC homozygous 957606241 3 120169245 120169246 G A 11 GENIC homozygous 957606242 3 120170196 120170197 T C 25 GENIC homozygous 957606243 3 120170329 120170330 T A 22 GENIC homozygous 957606244 3 120170624 120170625 T A 25 GENIC homozygous 957606245 3 120171741 120171742 C T 32 GENIC homozygous 957606246 3 120173445 120173446 T A 29 GENIC homozygous 957606247 3 120173873 120173874 C T 35 GENIC possibly homozygous 957606248 3 120174108 120174109 G A 10 GENIC possibly homozygous 957606249 3 120174129 120174130 G T 12 GENIC heterozygous 957606250 3 120175532 120175533 T C 27 GENIC homozygous 957606251 3 120176037 120176038 A G 24 GENIC homozygous 957606252 3 120176096 120176097 C T 28 GENIC homozygous 957606253 3 120176477 120176478 G A 32 GENIC homozygous 957606254 3 120176667 120176668 C A 36 GENIC homozygous 957606255 3 120176735 120176736 C T 30 GENIC homozygous 957606256 3 120177822 120177823 C T 43 GENIC homozygous 957606257 3 120178300 120178301 G T 28 GENIC homozygous 957606258 3 120178317 120178318 T G 24 GENIC homozygous 957606259 3 120178503 120178504 G A 32 GENIC homozygous 957606260 3 120178581 120178582 T G 28 GENIC homozygous 957606261 3 120179266 120179267 C A 30 GENIC homozygous 957606262 3 120179283 120179284 T A 25 GENIC homozygous 957606263 3 120179759 120179760 G A 14 GENIC homozygous 957606264 3 120179772 120179773 C T 17 GENIC homozygous 957606265 3 120179787 120179788 A C 20 GENIC homozygous 957606266 3 120181331 120181332 G C 31 GENIC homozygous 957606267 3 120181983 120181984 C T 16 GENIC homozygous 957606268