chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 123900994 123900995 A G 7 GENIC homozygous 986856809 X 123901333 123901334 T C 12 GENIC homozygous 986856810 X 123901666 123901667 C A 10 GENIC homozygous 986856811 X 123902771 123902772 C T 11 GENIC homozygous 986856812 X 123903040 123903041 C T 8 GENIC homozygous 986856813 X 123903719 123903720 T A 11 GENIC homozygous 986856814 X 123904886 123904887 A C 10 GENIC homozygous 986856815 X 123904966 123904967 G A 10 GENIC homozygous 986856816 X 123905627 123905628 A G 8 GENIC homozygous 986856817 X 123906808 123906809 A G 10 GENIC homozygous 986856818 X 123906932 123906933 T A 7 GENIC homozygous 986856819 X 123907599 123907600 C T 6 GENIC homozygous 986856820 X 123909136 123909137 C G 10 GENIC homozygous 986856821 X 123911321 123911322 T C 7 INTERGENIC homozygous 986856822 X 123911461 123911462 G T 16 INTERGENIC homozygous 986856823 X 123911482 123911483 G A 11 INTERGENIC homozygous 986856824 X 123911483 123911484 T G 10 INTERGENIC homozygous 986856825 X 123912197 123912198 T C 5 INTERGENIC homozygous 986856826 X 123914613 123914614 A G 7 INTERGENIC homozygous 986856827 X 123916196 123916197 A G 8 INTERGENIC homozygous 986856828 X 123916552 123916553 G A 11 INTERGENIC homozygous 986856829 X 123916936 123916937 A G 20 INTERGENIC homozygous 986856830