chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	97238288	97238289	G	GC	6	GENIC	heterozygous	51751133
10	97240242	97240243	C	-	6	GENIC	homozygous	51751136
10	97243376	97243378	GT	--	8	GENIC	heterozygous	52811701
10	97243525	97243526	T	TG	10	GENIC	homozygous	52400450
10	97249430	97249432	AC	--	7	GENIC	heterozygous	51556485
10	97257300	97257301	T	TAGGGTACTTGG	3	GENIC	homozygous	52400454
10	97261652	97261653	G	GGATA	3	GENIC	heterozygous	52651330
10	97264497	97264499	TG	--	10	GENIC	heterozygous	52446354
10	97269245	97269249	CCCC	----	7	GENIC	homozygous	52400458
10	97269248	97269249	C	CAAAA	7	GENIC	homozygous	52400460
10	97276769	97276770	A	AGATG	5	GENIC	heterozygous	51751168
10	97280869	97280870	T	C	21	GENIC	homozygous	51556593
10	97280888	97280889	C	-	12	GENIC	homozygous	51556594
10	97280893	97280894	C	-	12	GENIC	homozygous	51556595
10	97282826	97282828	CA	--	1	GENIC	homozygous	52400470
10	97284287	97284288	G	GA	17	GENIC	heterozygous	52604778
10	97290403	97290404	C	CT	8	GENIC	homozygous	51556605
10	97293949	97293953	AGAA	----	5	GENIC	homozygous	52400472
10	97295110	97295112	TC	--	4	GENIC	heterozygous	51556613