chr start stop reference nuc variant nuc depth genic status zygosity variant ID 2 193892863 193892864 T G 16 GENIC homozygous 110183845 2 193893000 193893001 T C 17 GENIC homozygous 110183846 2 193893328 193893329 A G 22 GENIC homozygous 110183847 2 193893449 193893450 C A 12 GENIC homozygous 110183848 2 193893652 193893653 G A 19 GENIC homozygous 110183849 2 193894139 193894140 T C 20 GENIC homozygous 110183850 2 193894296 193894297 T C 15 GENIC homozygous 110183851 2 193894778 193894779 A G 25 GENIC homozygous 110183852 2 193894864 193894865 A G 25 GENIC homozygous 110183853 2 193894986 193894987 T C 24 GENIC homozygous 110183854 2 193895345 193895346 T G 35 GENIC homozygous 110183855 2 193895806 193895807 A G 25 GENIC homozygous 110183856 2 193895931 193895932 G A 25 GENIC homozygous 110183857 2 193896189 193896190 A G 24 GENIC homozygous 110183858 2 193896653 193896654 C T 26 GENIC homozygous 110183859 2 193897031 193897032 C T 31 GENIC homozygous 110183860 2 193897173 193897174 C T 26 GENIC homozygous 110183861 2 193897380 193897381 T C 22 GENIC homozygous 110183862 2 193897626 193897627 T A 26 GENIC homozygous 110183863 2 193899775 193899776 C G 27 GENIC homozygous 110183864 2 193900300 193900301 A G 26 GENIC homozygous 110183865