chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	24317890	24317891	A	G	46	GENIC	homozygous	115287674
12	24319105	24319106	T	G	51	GENIC	homozygous	115287676
12	24319106	24319107	T	C	51	GENIC	homozygous	115287678
12	24320948	24320949	T	C	35	GENIC	homozygous	115287680
12	24321081	24321082	C	G	34	GENIC	homozygous	115287682
12	24321082	24321083	C	A	34	GENIC	homozygous	115287684
12	24321446	24321447	G	A	52	GENIC	homozygous	115287686
12	24322046	24322047	A	G	57	GENIC	homozygous	115287688
12	24322175	24322176	A	C	31	GENIC	homozygous	115287690
12	24322647	24322648	T	C	31	GENIC	homozygous	115287692
12	24324702	24324703	C	T	17	GENIC	homozygous	115287694
12	24325383	24325384	A	T	38	GENIC	homozygous	115287696
12	24325794	24325795	A	C	42	GENIC	homozygous	115287698
12	24325890	24325891	T	C	46	GENIC	homozygous	115287700
12	24326667	24326668	T	C	46	GENIC	homozygous	115287702
12	24326982	24326983	C	T	49	GENIC	homozygous	115287704
12	24328100	24328101	C	G	38	GENIC	homozygous	115287706
12	24328922	24328923	T	C	31	GENIC	homozygous	115287708
12	24329112	24329113	A	G	23	GENIC	homozygous	115287710
12	24329602	24329603	A	C	46	GENIC	homozygous	115287712
12	24331293	24331294	G	T	36	GENIC	homozygous	115287714
12	24332137	24332138	T	C	46	GENIC	homozygous	115287716
12	24335868	24335869	C	T	30	GENIC	homozygous	115287718
12	24336864	24336865	T	C	42	GENIC	homozygous	115287720
12	24337522	24337523	C	A	49	GENIC	homozygous	115287722