chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	36880033	36880033		TTG	33	GENIC	homozygous	142313778
12	36882411	36882413	AC		30	GENIC	heterozygous	142313779
12	36882649	36882655	GGGGTG		14	GENIC	homozygous	144914744
12	36882958	36882960	AT		20	GENIC	heterozygous	144914745
12	36880070	36880071	T		30	GENIC	homozygous	139054159
12	36881853	36881854	T	C	72	GENIC	heterozygous	154739304
12	36881853	36881854	T	G	72	GENIC	homozygous	154739305
12	36882959	36882960	T	C	20	GENIC	heterozygous	154739306
12	36882959	36882960	T		20	GENIC	heterozygous	403326317
12	36888135	36888136	T	C	35	GENIC	homozygous	139137584
12	36882592	36882593	C	A	31	GENIC	homozygous	139137583
12	36883947	36883948	G	A	61	GENIC	homozygous	142338000
12	36884342	36884343	G	C	54	GENIC	homozygous	142338001
12	36889965	36889966	C	T	49	GENIC	homozygous	139137586
12	36889971	36889972	C	T	49	GENIC	homozygous	142338002
12	36890215	36890216	G	A	38	GENIC	homozygous	142338003
12	36890825	36890826	A	G	48	GENIC	homozygous	139137587
12	36891298	36891299	G	A	38	GENIC	homozygous	142338004
12	36891571	36891572	T	C	49	GENIC	homozygous	142338005
12	36893524	36893524		A	32	GENIC	homozygous	142313781
12	36894093	36894094	A	G	59	GENIC	homozygous	142338009
12	36891782	36891783	A	G	55	GENIC	homozygous	142338006
12	36892223	36892224	G	A	57	GENIC	homozygous	142338007
12	36893380	36893381	G	C	43	GENIC	homozygous	142338008
12	36891056	36891057	G	A	17	GENIC	homozygous	144923679
12	36894415	36894416	C	T	50	GENIC	homozygous	142338010
12	36894807	36894808	C	T	56	GENIC	homozygous	139137591