chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	24319105	24319106	T	G	14	GENIC	homozygous	115287676
12	24319106	24319107	T	C	15	GENIC	homozygous	115287678
12	24319918	24319919	G	A	18	GENIC	homozygous	115598675
12	24320031	24320032	T	A	18	GENIC	homozygous	115422192
12	24320324	24320325	C	T	30	GENIC	homozygous	115470143
12	24320830	24320831	A	G	11	GENIC	homozygous	115493071
12	24321081	24321082	C	G	23	GENIC	homozygous	115287682
12	24321082	24321083	C	A	23	GENIC	homozygous	115287684
12	24322046	24322047	A	G	12	GENIC	homozygous	115287688
12	24322647	24322648	T	C	26	GENIC	homozygous	115287692
12	24325383	24325384	A	T	20	GENIC	homozygous	115287696
12	24326667	24326668	T	C	18	GENIC	homozygous	115287702
12	24328100	24328101	C	G	25	GENIC	homozygous	115287706
12	24328922	24328923	T	C	21	GENIC	homozygous	115287708
12	24329112	24329113	A	G	25	GENIC	homozygous	115287710
12	24329602	24329603	A	C	18	GENIC	homozygous	115287712
12	24331293	24331294	G	T	21	GENIC	homozygous	115287714
12	24332137	24332138	T	C	17	GENIC	homozygous	115287716
12	24332553	24332554	G	A	33	GENIC	homozygous	115598677
12	24335072	24335073	G	A	13	GENIC	homozygous	115598679
12	24335441	24335442	C	T	23	GENIC	homozygous	115598681
12	24336012	24336013	G	A	13	GENIC	homozygous	115598683
12	24336150	24336151	G	A	16	GENIC	homozygous	115422198
12	24336864	24336865	T	C	12	GENIC	homozygous	115287720
12	24337522	24337523	C	A	25	GENIC	homozygous	115287722