chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 123900994 123900995 A G 9 GENIC homozygous 814718330 X 123901333 123901334 T C 9 GENIC homozygous 814718331 X 123901666 123901667 C A 8 GENIC homozygous 814718332 X 123901786 123901787 C G 6 GENIC homozygous 814718333 X 123902364 123902365 T C 18 GENIC homozygous 814718334 X 123902771 123902772 C T 14 GENIC homozygous 814718335 X 123903040 123903041 C T 23 GENIC homozygous 814718336 X 123903719 123903720 T A 16 GENIC homozygous 814718337 X 123904966 123904967 G A 16 GENIC homozygous 814718338 X 123905627 123905628 A G 11 GENIC homozygous 814718339 X 123906352 123906353 G T 14 GENIC homozygous 814718340 X 123906932 123906933 T A 2 GENIC homozygous 814718341 X 123907599 123907600 C T 16 GENIC homozygous 814718342 X 123907796 123907797 C T 14 GENIC homozygous 814718343 X 123907829 123907830 T C 9 GENIC homozygous 814718344 X 123907913 123907914 C G 3 GENIC homozygous 814718345 X 123908139 123908140 A G 23 GENIC heterozygous 814718346 X 123909136 123909137 C G 17 GENIC homozygous 814718347 X 123910070 123910071 T G 16 GENIC homozygous 814718348 X 123910074 123910075 G A 17 GENIC homozygous 814718349 X 123910082 123910083 A G 18 GENIC homozygous 814718350 X 123910759 123910760 A C 5 GENIC homozygous 814718351 X 123910765 123910766 T G 7 GENIC homozygous 814718352 X 123910855 123910856 C T 10 GENIC homozygous 814718353 X 123910914 123910915 T A 8 GENIC homozygous 814718354 X 123911112 123911113 G T 5 GENIC homozygous 814718355 X 123911193 123911194 A T 8 GENIC homozygous 814718356 X 123911287 123911288 T G 15 GENIC homozygous 814718357 X 123911321 123911322 T C 14 GENIC homozygous 814718358 X 123911461 123911462 G T 8 GENIC homozygous 814718359 X 123912197 123912198 T C 17 GENIC homozygous 814718360 X 123914613 123914614 A G 6 GENIC homozygous 814718361 X 123916196 123916197 A G 13 GENIC homozygous 814718362 X 123916552 123916553 G A 10 GENIC homozygous 814718363 X 123916936 123916937 A G 9 GENIC homozygous 814718364