chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	24317890	24317891	A	G	30	GENIC	homozygous	115287674
12	24319105	24319106	T	G	21	GENIC	homozygous	115287676
12	24319106	24319107	T	C	21	GENIC	homozygous	115287678
12	24320948	24320949	T	C	14	GENIC	homozygous	115287680
12	24321081	24321082	C	G	17	GENIC	homozygous	115287682
12	24321082	24321083	C	A	17	GENIC	homozygous	115287684
12	24321446	24321447	G	A	8	GENIC	homozygous	115287686
12	24322046	24322047	A	G	27	GENIC	homozygous	115287688
12	24322175	24322176	A	C	11	GENIC	homozygous	115287690
12	24322647	24322648	T	C	18	GENIC	homozygous	115287692
12	24324702	24324703	C	T	16	GENIC	homozygous	115287694
12	24325383	24325384	A	T	20	GENIC	homozygous	115287696
12	24325794	24325795	A	C	17	GENIC	homozygous	115287698
12	24326667	24326668	T	C	19	GENIC	homozygous	115287702
12	24326982	24326983	C	T	11	GENIC	homozygous	115287704
12	24328100	24328101	C	G	19	GENIC	homozygous	115287706
12	24318449	24318450	G	A	8	GENIC	homozygous	118262081
12	24320031	24320032	T	A	15	GENIC	homozygous	115422192
12	24325962	24325963	G		15	GENIC	homozygous	128973265
12	24328922	24328923	T	C	12	GENIC	homozygous	115287708
12	24329112	24329113	A	G	18	GENIC	homozygous	115287710
12	24329602	24329603	A	C	21	GENIC	homozygous	115287712
12	24331293	24331294	G	T	21	GENIC	homozygous	115287714
12	24332137	24332138	T	C	22	GENIC	homozygous	115287716
12	24335868	24335869	C	T	14	GENIC	homozygous	115287718
12	24336150	24336151	G	A	19	GENIC	homozygous	115422198
12	24336180	24336181	C	T	17	GENIC	homozygous	115422200
12	24336864	24336865	T	C	21	GENIC	homozygous	115287720
12	24337522	24337523	C	A	20	GENIC	homozygous	115287722
12	24338715	24338715		ACAC	17	GENIC	homozygous	128973266
12	24339286	24339286		GGAGCTGGGGGTTAGTGTGATAACAGTCTGGTCTCTAACTCTTCTATCTCCCCTTCAGGAGCTGGGGGTTGGTGTGATAACAGTCTGGTCTCTAACTCTTCTATCTCCCCTTCA	16	GENIC	homozygous	128973267
12	24341090	24341091	C	T	11	GENIC	homozygous	115422204