chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 123900994 123900995 A G 16 GENIC homozygous 936924382 X 123901333 123901334 T C 16 GENIC homozygous 936924383 X 123901666 123901667 C A 9 GENIC homozygous 936924384 X 123902771 123902772 C T 13 GENIC homozygous 936924385 X 123903040 123903041 C T 11 GENIC homozygous 936924386 X 123903719 123903720 T A 15 GENIC homozygous 936924387 X 123904886 123904887 A C 11 GENIC homozygous 936924388 X 123904966 123904967 G A 6 GENIC homozygous 936924389 X 123905627 123905628 A G 6 GENIC homozygous 936924390 X 123906352 123906353 G T 12 GENIC homozygous 936924391 X 123906808 123906809 A G 14 GENIC homozygous 936924392 X 123906932 123906933 T A 24 GENIC homozygous 936924393 X 123907599 123907600 C T 9 GENIC homozygous 936924394 X 123909136 123909137 C G 11 GENIC homozygous 936924395 X 123911461 123911462 G T 11 INTERGENIC homozygous 936924396 X 123911482 123911483 G A 13 INTERGENIC homozygous 936924397 X 123911483 123911484 T G 12 INTERGENIC homozygous 936924398 X 123912197 123912198 T C 9 INTERGENIC homozygous 936924399 X 123914613 123914614 A G 18 INTERGENIC homozygous 936924400 X 123916196 123916197 A G 13 INTERGENIC homozygous 936924401 X 123916552 123916553 G A 17 INTERGENIC homozygous 936924402 X 123916936 123916937 A G 14 INTERGENIC homozygous 936924403