chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	123054915	123054917	TT	--	16	GENIC	heterozygous	54587240
7	123054916	123054917	T	-	16	GENIC	heterozygous	54088980
7	123055025	123055026	C	T	25	GENIC	homozygous	54088981
7	123056263	123056264	G	T	21	GENIC	homozygous	54088982
7	123057160	123057161	C	T	24	GENIC	homozygous	54088983
7	123057325	123057326	C	-	28	GENIC	homozygous	54088984
7	123058614	123058616	GT	--	10	GENIC	homozygous	54088985
7	123058634	123058638	GTGT	----	11	GENIC	homozygous	55144898
7	123058655	123058656	T	C	11	GENIC	homozygous	55144899
7	123058683	123058684	T	C	11	GENIC	homozygous	54088987
7	123059887	123060006	CAGAGACTTTTTTTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGGGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCC	-----------------------------------------------------------------------------------------------------------------------	33	GENIC	homozygous	54921391
7	123060720	123060721	T	TCC	11	GENIC	homozygous	55097002
7	123060748	123060749	G	GGAAA	11	GENIC	possibly homozygous	54088989
7	123061640	123061641	G	A	22	GENIC	homozygous	54088990
7	123061668	123061669	T	A	24	GENIC	homozygous	54088991
7	123061678	123061679	G	-	23	GENIC	homozygous	54088992
7	123062753	123062754	A	-	18	GENIC	homozygous	54235785
7	123063533	123063534	C	T	15	GENIC	homozygous	54088993