chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	135963921	135963922	A	G	27	GENIC	homozygous	114018740
5	135965311	135965312	A	G	15	GENIC	homozygous	114018743
5	135965675	135965676	G	T	18	GENIC	homozygous	114018744
5	135966183	135966184	A	T	5	GENIC	homozygous	114018745
5	135966324	135966325	G	C	20	GENIC	heterozygous	126204630
5	135968347	135968348	T	C	13	GENIC	homozygous	114018747
5	135968788	135968789	C	T	12	GENIC	homozygous	114018748
5	135969112	135969113	A	G	13	GENIC	homozygous	114018749
5	135969913	135969914	T	C	18	GENIC	homozygous	114018750
5	135972981	135972982	G	T	16	GENIC	homozygous	114018753
5	135974978	135974979	A	G	20	GENIC	homozygous	114018755
5	135975465	135975466	C	T	25	GENIC	homozygous	126204631
5	135975514	135975515	C	T	27	GENIC	homozygous	126204632
5	135977712	135977713	T	C	4	GENIC	homozygous	126204633
5	135977755	135977756	C	G	16	GENIC	homozygous	126204634
5	135977808	135977809	C	T	20	GENIC	homozygous	114018756
5	135977966	135977967	G	A	23	GENIC	homozygous	114018757
5	135978092	135978093	C	T	25	GENIC	homozygous	114018758
5	135980630	135980631	C	T	19	GENIC	homozygous	114018759
5	135980996	135980997	A	G	14	GENIC	homozygous	114018760
5	135982627	135982628	A	G	22	GENIC	homozygous	114018762
5	135982678	135982679	A	G	12	GENIC	homozygous	114018763
5	135982688	135982689	A	T	12	GENIC	homozygous	114018764