chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	230472827	230472828	C	T	33	GENIC	homozygous	59431943
2	230473512	230473513	C	T	26	GENIC	homozygous	59431944
2	230473813	230473814	C	T	24	GENIC	homozygous	59431945
2	230473897	230473898	A	G	12	GENIC	homozygous	59431946
2	230473898	230473899	C	G	12	GENIC	homozygous	59431947
2	230474730	230474731	G	A	37	GENIC	homozygous	59431949
2	230475825	230475826	G	A	21	GENIC	homozygous	59431951
2	230476295	230476296	T	-	13	GENIC	homozygous	59431952
2	230476539	230476540	C	CCA	3	GENIC	heterozygous	60520653
2	230477143	230477144	C	T	26	GENIC	homozygous	59431953
2	230477381	230477382	G	A	23	GENIC	homozygous	59431954
2	230477500	230477501	T	C	24	GENIC	homozygous	59431955
2	230477896	230477897	A	AG	30	GENIC	homozygous	59431956
2	230478593	230478594	A	G	37	GENIC	homozygous	59431957
2	230479347	230479348	A	G	8	GENIC	homozygous	59431959
2	230479988	230479989	A	T	25	GENIC	homozygous	59431961
2	230480119	230480120	G	C	17	GENIC	homozygous	59431962
2	230480287	230480288	T	C	26	GENIC	homozygous	59431963
2	230480429	230480430	T	C	31	GENIC	homozygous	59431964
2	230480682	230480683	T	C	29	GENIC	homozygous	59431965
2	230480871	230480872	A	C	15	GENIC	homozygous	59431966
2	230481238	230481239	C	T	9	GENIC	homozygous	59431967
2	230482198	230482199	T	C	32	GENIC	homozygous	59431968
2	230482668	230482669	A	G	36	GENIC	homozygous	59431969
2	230482731	230482732	C	CTTCATTCA	21	GENIC	homozygous	59431970
2	230483192	230483193	A	G	28	GENIC	homozygous	59431971
2	230483236	230483237	T	C	23	GENIC	homozygous	59431972
2	230483327	230483328	C	T	23	GENIC	homozygous	59431973
2	230483472	230483473	G	A	25	GENIC	homozygous	59431974
2	230483797	230483798	G	A	25	GENIC	homozygous	59431975
2	230484491	230484492	C	T	28	GENIC	homozygous	59431976
2	230484580	230484581	G	A	30	GENIC	homozygous	59431977
2	230484922	230484923	T	C	47	GENIC	homozygous	59431978
2	230486073	230486077	TTCA	----	22	GENIC	homozygous	59431979
2	230486117	230486118	T	C	21	GENIC	homozygous	59431981