chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 124723280 124723281 T C 10 GENIC homozygous 108326267 X 124725082 124725083 A G 15 GENIC homozygous 108326273 X 124725898 124725899 C G 12 GENIC homozygous 108424725 X 124726205 124726206 G A 12 GENIC homozygous 108326275 X 124731973 124731974 A C 7 GENIC homozygous 108326277 X 124741491 124741492 T C 6 GENIC homozygous 108326281 X 124742681 124742682 A G 15 GENIC homozygous 108424727 X 124743427 124743428 A C 20 GENIC homozygous 108326283 X 124743935 124743936 A G 9 GENIC homozygous 108326285 X 124745634 124745635 T C 20 GENIC homozygous 108326289 X 124746866 124746867 C T 4 GENIC homozygous 108326291 X 124747331 124747332 G A 7 GENIC homozygous 108326293 X 124748552 124748553 T A 25 GENIC homozygous 108326295 X 124749078 124749079 G A 16 GENIC homozygous 108326297 X 124753199 124753200 G A 14 GENIC homozygous 108326305 X 124753405 124753406 C T 9 GENIC homozygous 108326307 X 124757222 124757223 T G 6 GENIC homozygous 108326309 X 124757735 124757736 A G 11 GENIC homozygous 108326311 X 124759581 124759582 C T 7 GENIC homozygous 108326313 X 124759853 124759854 C T 10 GENIC homozygous 108326315 X 124760647 124760648 T A 12 GENIC homozygous 108326317 X 124761379 124761380 G A 17 GENIC homozygous 108326319 X 124765719 124765720 T C 2 GENIC homozygous 108767327