chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 24103800 24103801 T G 16 GENIC homozygous 945017900 14 24103859 24103860 T A 21 GENIC homozygous 945017901 14 24104271 24104272 T C 30 GENIC homozygous 945017902 14 24104367 24104368 T C 33 GENIC homozygous 945017903 14 24104416 24104417 G C 23 GENIC homozygous 945017904 14 24104564 24104565 G A 32 GENIC homozygous 945017905 14 24104718 24104719 G A 13 GENIC homozygous 945017906 14 24104742 24104743 T C 17 GENIC homozygous 945017907 14 24106695 24106696 G A 14 GENIC homozygous 945017908 14 24109614 24109615 T C 21 GENIC homozygous 945017909 14 24109642 24109643 C T 24 GENIC homozygous 945017910 14 24109823 24109824 G T 41 GENIC homozygous 945017911 14 24109894 24109895 G T 27 GENIC homozygous 945017912 14 24109990 24109991 G C 29 GENIC homozygous 945017913 14 24116537 24116538 T C 29 GENIC homozygous 945017914 14 24116710 24116711 G A 23 GENIC homozygous 945017915 14 24117045 24117046 A C 40 GENIC homozygous 945017916 14 24119438 24119439 T A 41 GENIC homozygous 945017917 14 24119888 24119889 G A 33 GENIC homozygous 945017918 14 24121237 24121238 G A 23 GENIC homozygous 945017919 14 24121487 24121488 G A 30 GENIC homozygous 945017920 14 24121869 24121870 A T 35 GENIC homozygous 945017921 14 24123292 24123293 G T 36 GENIC homozygous 945017922 14 24123313 24123314 G C 37 GENIC homozygous 945017923 14 24123891 24123892 G C 31 GENIC homozygous 945017924 14 24125242 24125243 T C 20 GENIC homozygous 945017925