chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	39214305	39214306	G	C	42	GENIC	heterozygous	118065799
10	39214318	39214319	T	C	45	GENIC	heterozygous	118065800
10	39214415	39214416	T	C	31	GENIC	heterozygous	117989751
10	39214430	39214431	T	C	31	GENIC	homozygous	117989752
10	39214498	39214499	T	C	40	GENIC	heterozygous	117989753
10	39214598	39214599	T	C	41	GENIC	heterozygous	117989754
10	39214604	39214605	C	T	37	GENIC	heterozygous	117989755
10	39214719	39214720	G		22	GENIC	heterozygous	128808754
10	39214721	39214722	A	T	22	GENIC	heterozygous	123344053
10	39214817	39214818	T		41	GENIC	heterozygous	128808755
10	39214827	39214828	A	C	43	GENIC	heterozygous	117277730
10	39214885	39214886	T	C	47	GENIC	heterozygous	116566513
10	39214900	39214901	G	C	43	GENIC	heterozygous	117277732
10	39215121	39215122	A	T	30	GENIC	heterozygous	123344056
10	39215122	39215123	G	A	30	GENIC	heterozygous	123344057
10	39215156	39215159	CTT		26	GENIC	heterozygous	128808756
10	39215303	39215304	A	G	30	GENIC	heterozygous	117217674
10	39215313	39215315	TC		29	GENIC	heterozygous	128808757
10	39215322	39215324	TG		30	GENIC	heterozygous	128808758
10	39215327	39215327		AC	29	GENIC	heterozygous	128808759
10	39215349	39215350	C	T	28	GENIC	heterozygous	118035308
10	39225591	39225592	T	C	27	GENIC	homozygous	116566535
10	39228049	39228050	A	G	20	GENIC	homozygous	116566549
10	39215261	39215262	T	C	27	GENIC	heterozygous	116763000
10	39215267	39215268	A	G	27	GENIC	heterozygous	116763002