chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	24654837	24654838	G	T	31	GENIC	possibly homozygous	50135529
12	24654848	24654849	G	A	27	GENIC	homozygous	50135531
12	24655193	24655194	C	T	42	GENIC	homozygous	50135533
12	24655293	24655294	G	A	26	GENIC	homozygous	50135535
12	24655472	24655473	G	A	29	GENIC	homozygous	50135538
12	24656294	24656295	A	G	43	GENIC	homozygous	50135540
12	24656863	24656864	T	TC	17	GENIC	homozygous	50135542
12	24656871	24656872	C	CA	20	GENIC	homozygous	50135544
12	24657204	24657205	A	G	14	GENIC	heterozygous	50135546
12	24657216	24657218	TC	--	11	GENIC	heterozygous	50135548
12	24657269	24657271	GG	--	8	GENIC	homozygous	50135550
12	24657523	24657524	G	A	34	GENIC	homozygous	50135552
12	24657613	24657614	G	A	29	GENIC	homozygous	50135554
12	24657705	24657706	G	A	18	GENIC	homozygous	50135556
12	24657767	24657768	C	T	22	GENIC	homozygous	50135558
12	24659370	24659371	T	C	19	GENIC	homozygous	50418495
12	24663134	24663135	G	A	13	GENIC	heterozygous	50135588
12	24663324	24663327	GGG	---	3	GENIC	heterozygous	50293536
12	24663512	24663513	C	T	22	GENIC	possibly homozygous	50135590
12	24663533	24663535	TT	--	26	GENIC	homozygous	50135592
12	24663538	24663539	T	G	28	GENIC	heterozygous	50135594
12	24663540	24663541	T	TG	27	GENIC	possibly homozygous	50135596