chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	49251624	49251625	T	C	52	GENIC	possibly homozygous	114616276
13	49252636	49252637	C	T	54	GENIC	homozygous	114616277
13	49252719	49252720	C	G	59	GENIC	homozygous	114616278
13	49253109	49253110	T	C	61	GENIC	homozygous	114616279
13	49253343	49253343		TC	45	GENIC	homozygous	132171746
13	49254009	49254010	T	A	54	GENIC	homozygous	114616280
13	49254233	49254234	G	C	55	GENIC	homozygous	114616281
13	49254857	49254858	G	A	55	GENIC	homozygous	114616282
13	49254955	49254956	T		42	GENIC	homozygous	132171747
13	49254974	49254974		TT	41	GENIC	homozygous	132171748
13	49255188	49255189	A	G	44	GENIC	homozygous	114616284
13	49255465	49255465		AAA	49	GENIC	homozygous	132171749
13	49258032	49258032		T	43	GENIC	possibly homozygous	132171750
13	49262786	49262787	C	T	36	GENIC	homozygous	114616286
13	49263024	49263024		G	10	GENIC	homozygous	132171751
13	49263092	49263093	T	C	19	GENIC	homozygous	114616287
13	49263262	49263263	T	C	48	GENIC	homozygous	114616288
13	49263516	49263517	C	T	38	GENIC	homozygous	114616289
13	49264044	49264045	A	G	46	GENIC	homozygous	114616290
13	49264193	49264194	T	A	38	GENIC	homozygous	114616291
13	49264780	49264781	G	T	48	GENIC	possibly homozygous	114616293
13	49264899	49264900	A	G	46	GENIC	homozygous	114616294
13	49266083	49266084	T	C	48	GENIC	homozygous	114871753
13	49268239	49268244	CTACA		50	GENIC	homozygous	132171752
13	49269054	49269055	C	A	53	GENIC	homozygous	114616296
13	49270080	49270081	G	A	58	GENIC	homozygous	114616297
13	49270415	49270416	A	T	48	GENIC	homozygous	114616299
13	49270760	49270761	A	G	27	GENIC	homozygous	118498082
13	49271594	49271594		T	7	GENIC	heterozygous	130690476
13	49271697	49271698	C		17	GENIC	homozygous	132171753
13	49271753	49271754	C	T	26	GENIC	homozygous	114616300
13	49273128	49273129	C	T	56	GENIC	homozygous	114616303
13	49273695	49273696	A	G	56	GENIC	homozygous	114616304