chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	42275520	42275521	C	T	22	GENIC	homozygous	144928925
13	42281047	42281047		A	41	GENIC	homozygous	144100549
13	42281395	42281396	T	C	33	GENIC	homozygous	144928926
13	42281455	42281456	C	T	38	GENIC	homozygous	144928927
13	42281473	42281473		GACA	39	GENIC	homozygous	144924538
13	42281841	42281842	C	T	49	GENIC	homozygous	144928928
13	42282867	42282868	A	C	25	GENIC	possibly homozygous	144928929
13	42282879	42282880	C		26	GENIC	heterozygous	144924539
13	42282882	42282883	C		26	GENIC	heterozygous	144924540
13	42282882	42282883	C	A	26	GENIC	heterozygous	154811077
13	42283301	42283302	T	G	44	GENIC	possibly homozygous	144928930
13	42283479	42283480	C	T	72	GENIC	homozygous	144928931
13	42283891	42283892	C	A	49	GENIC	homozygous	144928932
13	42284526	42284527	G	T	36	GENIC	homozygous	144928933
13	42284854	42284855	T		14	GENIC	heterozygous	144924541
13	42284854	42284855	T	G	14	GENIC	homozygous	154811078
13	42285675	42285676	A	T	34	GENIC	homozygous	144928934
13	42286277	42286278	C	T	52	GENIC	homozygous	144928935