chr start stop reference nuc variant nuc depth genic status zygosity variant ID 17 16430025 16430026 T C 25 GENIC homozygous 110970170 17 16430052 16430053 A T 24 GENIC homozygous 110970172 17 16430468 16430469 A G 32 GENIC homozygous 110970174 17 16431488 16431489 G T 27 GENIC homozygous 110970176 17 16431826 16431827 G T 16 GENIC homozygous 110970178 17 16432750 16432751 T C 17 GENIC homozygous 110970180 17 16432844 16432845 A G 22 GENIC homozygous 110970182 17 16433028 16433029 T G 22 GENIC homozygous 110970184 17 16433130 16433131 G A 19 GENIC homozygous 110970186 17 16433262 16433263 G A 21 GENIC homozygous 110970188 17 16433327 16433328 C G 19 GENIC homozygous 110970190 17 16434008 16434009 G A 19 GENIC homozygous 110970192 17 16435116 16435117 G A 25 GENIC homozygous 111173263 17 16433407 16433408 A T 23 GENIC homozygous 111173259 17 16434181 16434182 C T 18 GENIC homozygous 111173261 17 16436183 16436184 T G 29 GENIC homozygous 110970194 17 16437154 16437155 G A 27 GENIC homozygous 110970196 17 16437182 16437183 G A 24 GENIC homozygous 110970198 17 16437509 16437510 A G 26 GENIC homozygous 110970200 17 16438023 16438024 C T 32 GENIC homozygous 110970202 17 16438958 16438959 G A 30 GENIC homozygous 110970204 17 16440626 16440627 T G 38 GENIC homozygous 110970206 17 16440719 16440720 T G 38 GENIC homozygous 110970208 17 16441526 16441527 C G 30 GENIC homozygous 110970210 17 16442629 16442630 G T 22 GENIC homozygous 110970212