chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	91464437	91464438	C	T	45	GENIC	homozygous	141400959
2	91465099	91465100	A	G	47	GENIC	homozygous	141400960
2	91465449	91465449		GTGT	39	GENIC	homozygous	141329210
2	91465485	91465486	C	T	40	GENIC	homozygous	136215365
2	91465598	91465598		GTGTGTGTATGTGTGTGTATTCA	28	GENIC	homozygous	141329211
2	91466367	91466368	C	T	40	GENIC	homozygous	136215366
2	91466408	91466409	G	C	42	GENIC	homozygous	136215367
2	91469493	91469494	T	C	48	GENIC	homozygous	141400961
2	91471146	91471147	G	A	47	GENIC	homozygous	141400962
2	91476487	91476488	T	C	43	GENIC	homozygous	136215404
2	91476642	91476644	AC		35	GENIC	homozygous	141329212
2	91479782	91479783	A	G	32	GENIC	homozygous	136215406
2	91479841	91479842	C	T	25	GENIC	homozygous	136215407
2	91479843	91479846	ACA		25	GENIC	homozygous	141329213
2	91480442	91480443	A	G	40	GENIC	homozygous	136215408
2	91480828	91480828		T	51	GENIC	homozygous	135927734
2	91481020	91481021	G	A	33	GENIC	homozygous	136215409
2	91481938	91481939	T	G	29	GENIC	homozygous	136215410
2	91479910	91479911	G	A	28	GENIC	homozygous	141400963
2	91481536	91481537	G	A	47	GENIC	homozygous	141400964