chr start stop reference nuc variant nuc depth genic status zygosity variant ID X 124723280 124723281 T C 5 GENIC homozygous 108326267 X 124725082 124725083 A G 12 GENIC homozygous 108326273 X 124725898 124725899 C G 7 GENIC homozygous 108424725 X 124726205 124726206 G A 11 GENIC homozygous 108326275 X 124731973 124731974 A C 13 GENIC homozygous 108326277 X 124734856 124734857 C T 12 GENIC homozygous 108326279 X 124741491 124741492 T C 6 GENIC homozygous 108326281 X 124742681 124742682 A G 7 GENIC homozygous 108424727 X 124743427 124743428 A C 10 GENIC homozygous 108326283 X 124743935 124743936 A G 12 GENIC homozygous 108326285 X 124745634 124745635 T C 8 GENIC homozygous 108326289 X 124746866 124746867 C T 9 GENIC homozygous 108326291 X 124747331 124747332 G A 4 GENIC homozygous 108326293 X 124748552 124748553 T A 8 GENIC homozygous 108326295 X 124749078 124749079 G A 6 GENIC homozygous 108326297 X 124749205 124749205 ACCTGATGTCA 3 GENIC homozygous 129787177 X 124728537 124728538 A 5 GENIC homozygous 129787176 X 124750926 124750926 A 9 GENIC homozygous 129787178 X 124750979 124750979 T 7 GENIC homozygous 129787179 X 124751241 124751245 CACT 7 GENIC homozygous 129787180 X 124751246 124751248 AC 7 GENIC homozygous 129787181 X 124751249 124751250 G C 7 GENIC homozygous 108326303 X 124753199 124753200 G A 12 GENIC homozygous 108326305 X 124753405 124753406 C T 12 GENIC homozygous 108326307 X 124754472 124754473 A 4 GENIC heterozygous 129787182 X 124757222 124757223 T G 12 GENIC homozygous 108326309 X 124757735 124757736 A G 12 GENIC homozygous 108326311 X 124759581 124759582 C T 11 GENIC homozygous 108326313 X 124759853 124759854 C T 9 GENIC homozygous 108326315 X 124760647 124760648 T A 7 GENIC homozygous 108326317 X 124761379 124761380 G A 16 GENIC homozygous 108326319 X 124756799 124756800 A G 7 GENIC homozygous 108635320