chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	36880033	36880033		TTG	29	GENIC	homozygous	142313778
12	36880070	36880071	T		20	GENIC	homozygous	139054159
12	36881853	36881854	T	C	76	GENIC	heterozygous	154739304
12	36881853	36881854	T	G	76	GENIC	homozygous	154739305
12	36882411	36882413	AC		32	GENIC	homozygous	142313779
12	36882649	36882655	GGGGTG		10	GENIC	homozygous	144914744
12	36882959	36882960	T	C	17	GENIC	possibly homozygous	154739306
12	36889024	36889025	A		10	GENIC	heterozygous	403847057
12	36889024	36889025	A	G	10	GENIC	heterozygous	403847058
12	36889026	36889027	A	G	10	GENIC	heterozygous	404467586
12	36882592	36882593	C	A	30	GENIC	homozygous	139137583
12	36888135	36888136	T	C	41	GENIC	homozygous	139137584
12	36882959	36882960	T		17	GENIC	heterozygous	403326317
12	36883947	36883948	G	A	71	GENIC	homozygous	142338000
12	36884342	36884343	G	C	68	GENIC	homozygous	142338001
12	36888705	36888706	C	A	6	GENIC	heterozygous	404467584
12	36889026	36889027	A		10	GENIC	heterozygous	404467585
12	36889965	36889966	C	T	49	GENIC	homozygous	139137586
12	36889971	36889972	C	T	48	GENIC	homozygous	142338002
12	36890215	36890216	G	A	46	GENIC	homozygous	142338003
12	36890825	36890826	A	G	40	GENIC	homozygous	139137587
12	36891056	36891057	G	A	21	GENIC	homozygous	144923679
12	36891298	36891299	G	A	31	GENIC	homozygous	142338004
12	36891571	36891572	T	C	48	GENIC	homozygous	142338005
12	36891782	36891783	A	G	46	GENIC	homozygous	142338006
12	36892223	36892224	G	A	55	GENIC	homozygous	142338007
12	36893380	36893381	G	C	38	GENIC	homozygous	142338008
12	36893524	36893524		A	39	GENIC	possibly homozygous	142313781
12	36894093	36894094	A	G	49	GENIC	homozygous	142338009
12	36894415	36894416	C	T	57	GENIC	homozygous	142338010
12	36894807	36894808	C	T	64	GENIC	homozygous	139137591