chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	128632772	128632773	G	A	25	GENIC	homozygous	55894395
5	128632886	128632887	T	TC	21	GENIC	homozygous	55894396
5	128632987	128632988	C	T	34	GENIC	homozygous	55894397
5	128633193	128633194	C	T	27	GENIC	homozygous	55894398
5	128633202	128633203	C	T	24	GENIC	homozygous	55894399
5	128633213	128633214	G	C	22	GENIC	homozygous	55894400
5	128633231	128633232	G	C	20	GENIC	homozygous	55894401
5	128633465	128633466	C	T	27	GENIC	homozygous	55708150
5	128633605	128633606	C	T	26	GENIC	homozygous	55708152
5	128633859	128633860	T	TTTC	7	GENIC	heterozygous	55708158
5	128634094	128634095	C	G	37	GENIC	homozygous	55894402
5	128634159	128634160	A	G	35	GENIC	homozygous	55894403
5	128634411	128634412	G	A	27	GENIC	homozygous	55894404
5	128634525	128634526	T	C	25	GENIC	homozygous	55894405
5	128634710	128634712	AG	--	25	GENIC	homozygous	55894406
5	128634713	128634717	GCTA	----	28	GENIC	homozygous	55894407
5	128634765	128634766	T	C	31	GENIC	homozygous	55708160
5	128634858	128634859	C	CTTTAGGCCGATAAT	32	GENIC	homozygous	56493092
5	128634861	128634862	T	TTGGTACTGAGCCTTCC	30	GENIC	homozygous	56493093
5	128634899	128634900	A	G	28	GENIC	homozygous	55708162
5	128635283	128635284	T	C	34	GENIC	homozygous	55708166
5	128635580	128635581	C	T	30	GENIC	homozygous	55708168
5	128635752	128635753	A	G	24	GENIC	homozygous	55708170
5	128635761	128635762	G	A	30	GENIC	homozygous	55708172
5	128635852	128635853	A	G	43	GENIC	homozygous	55708174
5	128635871	128635872	G	C	42	GENIC	homozygous	55708176
5	128635963	128635964	A	G	34	GENIC	homozygous	55708178
5	128636181	128636182	C	T	34	GENIC	homozygous	55708180
5	128636485	128636486	G	A	26	GENIC	homozygous	55708182
5	128636610	128636611	T	-	19	GENIC	homozygous	55708184
5	128636648	128636649	A	C	28	GENIC	homozygous	55708186