chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	33892894	33892894		G	15	GENIC	homozygous	128020268
4	33892901	33892902	C		13	GENIC	homozygous	128020269
4	33892914	33892918	AAAG		13	GENIC	homozygous	128020270
4	33892918	33892919	A	C	13	GENIC	homozygous	122021680
4	33892920	33892921	A	G	14	GENIC	homozygous	113007137
4	33892941	33892942	A		14	GENIC	homozygous	128020271
4	33892942	33892943	A	G	15	GENIC	homozygous	122021682
4	33892948	33892948		T	15	GENIC	homozygous	128020272
4	33892981	33892992	AAAAAAAAAAA		12	GENIC	homozygous	128020273
4	33892994	33893003	CTATTACAA		12	GENIC	homozygous	128020274
4	33893006	33893010	AAAA		12	GENIC	homozygous	128020275
4	33893011	33893011		GGTGCTGCGGCGGG	12	GENIC	homozygous	128020276
4	33893017	33893018	A	C	11	GENIC	homozygous	122021688
4	33893019	33893020	C		11	GENIC	homozygous	128020277
4	33897790	33897796	CTTAGT		2	GENIC	homozygous	128020279
4	33897815	33897816	G	A	4	GENIC	heterozygous	130753635
4	33898252	33898253	T	C	9	GENIC	heterozygous	130753636
4	33892950	33892951	T	G	15	GENIC	homozygous	112573561
4	33893011	33893012	A	C	11	GENIC	homozygous	119475755
4	33893014	33893015	A	G	11	GENIC	homozygous	119497662