chr start stop reference nuc variant nuc depth genic status zygosity variant ID 12 23928990 23928991 A G 18 GENIC homozygous 115581675 12 23929276 23929277 T A 11 GENIC homozygous 115438568 12 23934909 23934910 C A 17 GENIC homozygous 115286165 12 23932395 23932396 A G 19 GENIC homozygous 115286157 12 23932517 23932518 A G 13 GENIC homozygous 115286159 12 23933452 23933453 C T 9 GENIC homozygous 115286161 12 23934283 23934284 A G 20 GENIC homozygous 115286163 12 23935174 23935175 T C 17 GENIC homozygous 115286167 12 23935180 23935181 G C 16 GENIC homozygous 115438571 12 23936264 23936265 T A 16 GENIC homozygous 115286169 12 23936390 23936391 C T 20 GENIC homozygous 115286171 12 23936432 23936433 T C 15 GENIC homozygous 115286173 12 23936687 23936688 T C 21 GENIC homozygous 115286175 12 23936688 23936689 C T 21 GENIC homozygous 115438573 12 23937094 23937095 C T 23 GENIC homozygous 115286177 12 23935822 23935823 A G 22 GENIC homozygous 115653533 12 23936091 23936092 T G 18 GENIC homozygous 115422060