chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	230368917	230368919	TG	--	10	GENIC	possibly homozygous	59431827
2	230370303	230370304	T	TTC	15	GENIC	homozygous	59431828
2	230370328	230370329	T	TC	19	GENIC	heterozygous	59431829
2	230370879	230370880	C	T	22	GENIC	homozygous	59431830
2	230376793	230376794	G	A	26	GENIC	homozygous	59431831
2	230379604	230379605	T	TTCATCATCA	8	GENIC	homozygous	59431832
2	230380529	230380530	C	T	39	GENIC	homozygous	59431834
2	230383135	230383136	T	C	28	GENIC	homozygous	59431835
2	230383623	230383627	AAAT	----	24	GENIC	homozygous	59431836
2	230384350	230384351	C	G	25	GENIC	homozygous	59431837
2	230386137	230386138	G	-	21	GENIC	heterozygous	59431838
2	230386140	230386141	C	T	30	GENIC	heterozygous	59431839
2	230389866	230389870	ACAC	----	16	GENIC	heterozygous	59431840
2	230389868	230389870	AC	--	16	GENIC	heterozygous	59431841
2	230391218	230391219	C	T	23	GENIC	homozygous	59431842
2	230393014	230393015	G	-	19	GENIC	homozygous	59431843
2	230394024	230394025	A	G	32	GENIC	homozygous	59431844
2	230394444	230394445	T	C	46	GENIC	possibly homozygous	59431845
2	230394477	230394478	T	C	34	GENIC	homozygous	59431846
2	230394866	230394867	C	CA	24	GENIC	homozygous	59431847
2	230395393	230395394	G	A	39	GENIC	homozygous	59431848
2	230398591	230398592	A	G	35	GENIC	homozygous	59431849
2	230399031	230399032	G	GGT	7	GENIC	possibly homozygous	59431850