chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	230368917	230368919	TG	--	10	GENIC	homozygous	59431827
2	230368962	230368963	T	G	18	GENIC	heterozygous	59775922
2	230370303	230370304	T	TTC	5	GENIC	homozygous	59431828
2	230370328	230370329	T	TCTCTCTCTC	6	GENIC	homozygous	59775923
2	230370328	230370330	TT	--	5	GENIC	heterozygous	60084993
2	230370879	230370880	C	T	54	GENIC	homozygous	59431830
2	230376793	230376794	G	A	38	GENIC	homozygous	59431831
2	230379604	230379605	T	TTCATCATCA	4	GENIC	homozygous	59431832
2	230380529	230380530	C	T	35	GENIC	homozygous	59431834
2	230383135	230383136	T	C	38	GENIC	homozygous	59431835
2	230383623	230383627	AAAT	----	33	GENIC	homozygous	59431836
2	230384350	230384351	C	G	44	GENIC	homozygous	59431837
2	230386137	230386138	G	-	28	GENIC	heterozygous	59431838
2	230389866	230389870	ACAC	----	9	GENIC	heterozygous	59431840
2	230389868	230389870	AC	--	9	GENIC	heterozygous	59431841
2	230391218	230391219	C	T	36	GENIC	homozygous	59431842
2	230393014	230393015	G	-	29	GENIC	homozygous	59431843
2	230394024	230394025	A	G	38	GENIC	homozygous	59431844
2	230394444	230394445	T	C	22	GENIC	possibly homozygous	59431845
2	230394477	230394478	T	C	27	GENIC	homozygous	59431846
2	230394866	230394867	C	CA	25	GENIC	homozygous	59431847
2	230395393	230395394	G	A	35	GENIC	homozygous	59431848
2	230398591	230398592	A	G	51	GENIC	homozygous	59431849