chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	47644395	47644396	G	A	34	GENIC	homozygous	114548321
13	47644449	47644450	G	A	38	GENIC	homozygous	114548322
13	47644605	47644606	T	C	47	GENIC	homozygous	114548323
13	47645152	47645153	T	C	47	GENIC	homozygous	114548324
13	47645582	47645582		TA	39	GENIC	homozygous	131501497
13	47645692	47645692		A	42	GENIC	possibly homozygous	131501498
13	47645761	47645762	G	A	45	GENIC	homozygous	114548325
13	47645990	47645991	A	G	47	GENIC	homozygous	114548326
13	47646370	47646372	AG		52	GENIC	homozygous	131501499
13	47646492	47646492		CCAGCATTTTATATTT	48	GENIC	homozygous	131501500
13	47647065	47647066	A	G	37	GENIC	homozygous	114548327
13	47648071	47648072	G	A	43	GENIC	homozygous	114548328
13	47648167	47648168	A	C	49	GENIC	homozygous	114548329
13	47648323	47648324	C	T	39	GENIC	homozygous	114548330
13	47649951	47649952	A		35	GENIC	homozygous	129050850
13	47649958	47649959	A		35	GENIC	homozygous	129050851
13	47650005	47650005		T	45	GENIC	homozygous	129050855
13	47649984	47649984		G	37	GENIC	homozygous	129050853
13	47649977	47649977		A	33	GENIC	homozygous	129050852
13	47649988	47649988		T	40	GENIC	homozygous	129050854
13	47650042	47650043	A		51	GENIC	homozygous	129050856
13	47650107	47650108	A	C	50	GENIC	homozygous	114548331
13	47650115	47650115		G	50	GENIC	homozygous	129050857
13	47650304	47650316	TCTGTCTCTCTC		6	GENIC	homozygous	131501501