chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	122665391	122665392	T	C	61	GENIC	homozygous	137607815
5	122666033	122666035	CT		53	GENIC	homozygous	143942520
5	122666478	122666479	T	C	67	GENIC	homozygous	137607816
5	122666716	122666717	C	T	58	GENIC	homozygous	137607817
5	122667283	122667284	C	A	59	GENIC	homozygous	137607818
5	122667600	122667601	G	A	58	GENIC	homozygous	137607819
5	122667667	122667668	T	C	63	GENIC	homozygous	137607820
5	122667900	122667901	C	T	78	GENIC	homozygous	137607821
5	122667997	122667998	C	T	69	GENIC	homozygous	137607822
5	122668191	122668192	G	A	60	GENIC	homozygous	137607823
5	122668375	122668376	A	C	72	GENIC	homozygous	137607824
5	122668509	122668510	T	G	65	GENIC	homozygous	137607825
5	122668774	122668775	G	A	69	GENIC	homozygous	137607826
5	122669051	122669052	C	T	53	GENIC	homozygous	137607827
5	122671038	122671038		C	59	GENIC	homozygous	137338021
5	122671117	122671118	G	A	48	GENIC	homozygous	137607829
5	122671236	122671237	C	T	34	GENIC	homozygous	137607830
5	122671517	122671518	G	C	69	GENIC	homozygous	137607831
5	122671863	122671864	A	G	61	GENIC	homozygous	137607832
5	122672027	122672028	T	C	33	GENIC	homozygous	137607833
5	122674416	122674417	G	T	57	GENIC	possibly homozygous	137607834
5	122676690	122676693	TCT		31	GENIC	possibly homozygous	143942521
5	122676706	122676724	CTTTCTCCTTTTCCTCCC		20	GENIC	homozygous	137338023
5	122676692	122676693	T		31	GENIC	possibly homozygous	403156019
5	122671564	122671565	A		59	GENIC	heterozygous	146122413
5	122671564	122671565	A	T	59	GENIC	possibly homozygous	154319241
5	122676692	122676693	T	C	31	GENIC	heterozygous	154319243