chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 11725291 11725292 G T 16 GENIC homozygous 116495335 10 11725577 11725578 G C 28 GENIC homozygous 116495337 10 11725899 11725900 G C 32 GENIC homozygous 116495339 10 11726840 11726841 G A 27 GENIC homozygous 116495341 10 11726856 11726857 C A 31 GENIC homozygous 116495343 10 11729903 11729904 G A 48 GENIC homozygous 116495345 10 11732330 11732331 C T 27 GENIC homozygous 116495347 10 11732827 11732828 G C 22 GENIC homozygous 116495349 10 11734826 11734827 C T 27 GENIC homozygous 116495351 10 11736722 11736723 G T 17 GENIC homozygous 116495353 10 11744399 11744400 A G 27 GENIC homozygous 116495355 10 11745814 11745815 T C 25 GENIC homozygous 116495357 10 11745827 11745828 T G 27 GENIC homozygous 116495359 10 11747302 11747303 T C 18 GENIC homozygous 116495361 10 11748710 11748711 G A 28 GENIC homozygous 116495363 10 11749510 11749511 T G 22 GENIC homozygous 116495365 10 11752717 11752718 A G 19 GENIC homozygous 116495367 10 11756255 11756256 A G 25 GENIC homozygous 116495369 10 11757029 11757030 A C 16 GENIC homozygous 116495371 10 11757452 11757453 T C 17 GENIC homozygous 116495373