chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	119474322	119474323	A	G	19	GENIC	homozygous	54081333
7	119474920	119474921	T	A	32	GENIC	homozygous	54859471
7	119474977	119474978	G	A	34	GENIC	homozygous	54859472
7	119476621	119476622	C	CTCCG	27	GENIC	homozygous	54081341
7	119477338	119477339	C	T	32	GENIC	homozygous	54859473
7	119479724	119479725	T	C	8	GENIC	homozygous	54081356
7	119481884	119481885	C	CTGTGTGTGTGTG	12	GENIC	homozygous	55001118
7	119483030	119483031	T	G	18	GENIC	homozygous	55001120
7	119485585	119485588	CAA	---	29	GENIC	homozygous	54081372
7	119486206	119486253	TGGAGGTGAGGATGGGGTGAGGTTAGAGGTGAGGATGGGGGTGAGGT	-----------------------------------------------	25	GENIC	heterozygous	55001122
7	119486291	119486413	GTGAGGGTGGAGGTGAGGATGGGGTGAGGATGGGGGGGAGGGTGTGAGGTTGGGGTGTGGGTGGGGTGAGGGTGGAGGTGAGGATGGGGTGAGAGTGGAGGTGAGGATGGGGTGAGGATGGG	--------------------------------------------------------------------------------------------------------------------------	28	GENIC	heterozygous	55001124
7	119487941	119487942	A	G	17	GENIC	homozygous	54081377
7	119489134	119489135	G	A	29	GENIC	homozygous	54859476
7	119489202	119489203	A	G	28	GENIC	homozygous	54081387
7	119489920	119489921	A	AAC	20	GENIC	possibly homozygous	54081389