chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	24720579	24720580	T	C	11	GENIC	possibly homozygous	50135970
12	24720595	24720596	T	C	11	GENIC	possibly homozygous	50135972
12	24720612	24720613	C	T	4	GENIC	homozygous	50508576
12	24720625	24720626	C	T	3	GENIC	homozygous	50508578
12	24720627	24720628	A	C	3	GENIC	homozygous	50135976
12	24720674	24720675	C	G	9	GENIC	homozygous	50508580
12	24720675	24720676	A	G	9	GENIC	homozygous	50135982
12	24720693	24720694	A	T	16	GENIC	homozygous	50508582
12	24720827	24720828	T	G	7	GENIC	possibly homozygous	50508584
12	24720896	24720897	C	CAA	12	GENIC	heterozygous	50508586
12	24720937	24720938	T	TCC	13	GENIC	homozygous	50508588
12	24720944	24720945	T	C	10	GENIC	homozygous	50508590
12	24720952	24720953	C	T	8	GENIC	homozygous	50508592
12	24721248	24721249	T	C	26	GENIC	possibly homozygous	50508594
12	24721320	24721321	C	A	9	GENIC	homozygous	50508596
12	24721321	24721322	T	C	9	GENIC	homozygous	50508598
12	24721338	24721339	A	G	16	GENIC	homozygous	50508600
12	24721524	24721525	A	G	13	GENIC	homozygous	50135992
12	24721936	24721937	G	A	9	GENIC	homozygous	50508603
12	24722229	24722230	G	A	15	GENIC	homozygous	50508605
12	24722303	24722304	T	C	25	GENIC	homozygous	50508608
12	24722478	24722479	G	A	19	GENIC	possibly homozygous	50508610
12	24722505	24722506	A	G	10	GENIC	homozygous	50508612
12	24722518	24722519	G	T	14	GENIC	homozygous	50508614
12	24722776	24722777	C	T	2	GENIC	homozygous	50508616
12	24722784	24722785	A	ACC	2	GENIC	homozygous	50508618
12	24722785	24722786	A	C	2	GENIC	homozygous	50508620
12	24722792	24722793	T	C	6	GENIC	homozygous	50508622
12	24722964	24722965	G	A	7	GENIC	homozygous	50508624
12	24722971	24722972	C	T	6	GENIC	heterozygous	50508626
12	24722972	24722973	A	G	6	GENIC	heterozygous	50508628
12	24723038	24723039	T	C	9	GENIC	possibly homozygous	50508630