chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	140092823	140092824	G	A	31	GENIC	homozygous	112855961
4	140094704	140094705	A	C	16	GENIC	homozygous	112855965
4	140094715	140094716	T	G	17	GENIC	homozygous	113174946
4	140094831	140094832	G	A	22	GENIC	homozygous	113174948
4	140095003	140095004	G	A	17	GENIC	homozygous	113174950
4	140096511	140096512	A	G	8	GENIC	homozygous	113174952
4	140096747	140096748	C	A	12	GENIC	homozygous	112855973
4	140097343	140097344	T	G	22	GENIC	homozygous	112855975
4	140097430	140097431	T	C	19	GENIC	homozygous	112855977
4	140097798	140097799	C	T	28	GENIC	homozygous	113174954
4	140097894	140097895	T	C	24	GENIC	homozygous	113174956
4	140098117	140098118	G	A	16	GENIC	homozygous	113174958
4	140098128	140098129	G	A	21	GENIC	homozygous	113174960
4	140098151	140098152	A	G	22	GENIC	homozygous	113174962
4	140098157	140098158	C	G	23	GENIC	homozygous	113174964
4	140098174	140098175	T	C	27	GENIC	homozygous	113174966
4	140098270	140098271	A	C	32	GENIC	homozygous	112855979
4	140098411	140098412	A	G	34	GENIC	homozygous	112855985
4	140098451	140098452	T	C	17	GENIC	homozygous	112855987
4	140098857	140098858	A	C	17	GENIC	homozygous	113174968
4	140098894	140098895	T	A	20	GENIC	homozygous	112855993
4	140099160	140099161	T	C	26	GENIC	homozygous	112855999
4	140099346	140099347	A	G	21	GENIC	homozygous	112856007
4	140100066	140100067	A	G	18	GENIC	homozygous	112856009
4	140100962	140100963	G	C	21	GENIC	homozygous	113174970
4	140101242	140101243	A	G	33	GENIC	homozygous	112856013
4	140103075	140103076	C	A	25	GENIC	homozygous	113174972
4	140103286	140103287	G	T	39	GENIC	homozygous	113174974
4	140103444	140103445	A	C	19	GENIC	homozygous	113174976
4	140103475	140103476	T	C	19	GENIC	homozygous	113174978
4	140104034	140104035	C	T	25	GENIC	homozygous	113174980