chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	13024128	13024129	C	A	28	GENIC	homozygous	53792468
7	13024976	13024977	A	-	8	GENIC	homozygous	54301910
7	13024993	13024994	C	CAAA	17	GENIC	homozygous	53792470
7	13026281	13026287	CACACA	------	15	GENIC	homozygous	56142749
7	13026620	13026621	G	A	37	GENIC	homozygous	56142752
7	13026707	13026708	C	T	42	GENIC	homozygous	56142754
7	13027520	13027521	G	GAAAA	17	GENIC	heterozygous	54301913
7	13027520	13027521	G	GAAA	17	GENIC	possibly homozygous	55057510
7	13030385	13030386	A	T	37	GENIC	homozygous	56142757
7	13031444	13031445	A	-	8	GENIC	heterozygous	56142760
7	13032324	13032325	C	T	30	GENIC	homozygous	56142763
7	13033232	13033233	T	C	19	GENIC	homozygous	53792478
7	13033481	13033482	T	C	31	GENIC	homozygous	53792479
7	13033933	13033934	G	A	19	GENIC	homozygous	56142766
7	13035704	13035705	C	CTTGGAGCAGT	48	GENIC	homozygous	53792480
7	13036346	13036347	C	G	32	GENIC	homozygous	53792482
7	13037149	13037150	A	G	15	GENIC	homozygous	53792484
7	13037169	13037170	G	GC	8	GENIC	homozygous	55126565
7	13037372	13037373	A	G	20	GENIC	homozygous	53792485
7	13037697	13037698	A	ATGTGTGTGTGTGTGTGTGTGTGTGTG	5	GENIC	homozygous	55391595
7	13039190	13039191	T	C	34	GENIC	homozygous	53792487
7	13041287	13041288	A	AC	15	GENIC	homozygous	53792489
7	13042528	13042529	A	ACCT	38	GENIC	homozygous	53792492
7	13042688	13042689	T	C	34	GENIC	homozygous	56142769
7	13042822	13042823	C	T	14	GENIC	possibly homozygous	56142772
7	13042856	13042857	T	C	14	GENIC	possibly homozygous	53792493
7	13043051	13043052	C	A	23	GENIC	homozygous	53792494
7	13043421	13043422	C	T	31	GENIC	possibly homozygous	53792495
7	13043696	13043697	A	G	30	GENIC	homozygous	53792496
7	13048476	13048477	C	CTT	37	GENIC	homozygous	56142775
7	13049007	13049008	G	A	29	GENIC	homozygous	56142778
7	13050526	13050527	C	T	35	GENIC	homozygous	56142781
7	13050774	13050775	T	C	28	GENIC	possibly homozygous	53792499