chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	230368917	230368919	TG	--	4	GENIC	homozygous	59431827
2	230368962	230368963	T	TTGTGTGTGTGTGTG	8	GENIC	homozygous	60520636
2	230370328	230370329	T	TCTCTCTCTC	2	GENIC	homozygous	59775923
2	230370879	230370880	C	T	22	GENIC	homozygous	59431830
2	230376793	230376794	G	A	29	GENIC	homozygous	59431831
2	230379604	230379605	T	TTCATCATCA	8	GENIC	possibly homozygous	59431832
2	230379604	230379605	T	TTCA	8	GENIC	heterozygous	60562137
2	230379740	230379741	C	CAAAAAAAAAAAAA	9	GENIC	homozygous	60458944
2	230380529	230380530	C	T	20	GENIC	possibly homozygous	59431834
2	230383135	230383136	T	C	23	GENIC	homozygous	59431835
2	230383623	230383627	AAAT	----	2	GENIC	homozygous	59431836
2	230384350	230384351	C	G	30	GENIC	homozygous	59431837
2	230386113	230386114	C	CTTTTTTTTTT	7	GENIC	homozygous	60520637
2	230389865	230389866	T	TAC	9	GENIC	heterozygous	60550454
2	230389866	230389868	AC	--	9	GENIC	possibly homozygous	60550456
2	230391218	230391219	C	T	29	GENIC	homozygous	59431842
2	230393014	230393015	G	-	18	GENIC	homozygous	59431843
2	230394024	230394025	A	G	21	GENIC	homozygous	59431844
2	230394444	230394445	T	C	17	GENIC	homozygous	59431845
2	230394477	230394478	T	C	17	GENIC	homozygous	59431846
2	230394866	230394867	C	CA	12	GENIC	homozygous	59431847
2	230395393	230395394	G	A	27	GENIC	homozygous	59431848
2	230398591	230398592	A	G	22	GENIC	homozygous	59431849