chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	103762374	103762375	T	C	21	GENIC	homozygous	115144695
6	103762449	103762450	T	A	45	GENIC	possibly homozygous	115144696
6	103762464	103762465	G	A	50	GENIC	possibly homozygous	115144697
6	103762475	103762476	C	G	56	GENIC	heterozygous	115144698
6	103762535	103762536	G	T	31	GENIC	homozygous	115144699
6	103762573	103762574	C	T	17	GENIC	homozygous	115503899
6	103762613	103762614	C	A	50	GENIC	homozygous	115144700
6	103762734	103762735	C	T	95	GENIC	possibly homozygous	115144701
6	103762815	103762816	C	G	63	GENIC	heterozygous	115519723
6	103762834	103762835	C	T	49	GENIC	heterozygous	115144702
6	103762948	103762949	G	C	14	GENIC	homozygous	115144703
6	103762992	103762993	A	C	4	GENIC	homozygous	115144704
6	103763050	103763051	C	G	7	GENIC	homozygous	115144705
6	103763059	103763060	C	T	11	GENIC	homozygous	115144706
6	103763198	103763199	C	T	38	GENIC	homozygous	115144707
6	103763220	103763221	G	A	42	GENIC	homozygous	115144708