chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	13593637	13593638	T	C	20	GENIC	homozygous	109610032
2	13594082	13594083	A	C	32	GENIC	homozygous	111087983
2	13596086	13596087	T	C	16	GENIC	homozygous	111087985
2	13596361	13596362	T	C	37	GENIC	homozygous	111087987
2	13596842	13596843	G	A	28	GENIC	homozygous	111087989
2	13597259	13597260	A	C	13	GENIC	homozygous	111087991
2	13597558	13597559	A	G	17	GENIC	homozygous	111087993
2	13599879	13599880	T	G	23	GENIC	possibly homozygous	111087996
2	13600100	13600101	G	A	26	GENIC	homozygous	109610052
2	13600687	13600688	T	C	29	GENIC	homozygous	109610056
2	13601279	13601280	G	A	27	GENIC	homozygous	111087998
2	13601319	13601320	C	T	18	GENIC	homozygous	109610057
2	13601692	13601693	G	A	21	GENIC	homozygous	111088000
2	13601702	13601703	C	T	25	GENIC	homozygous	109610058
2	13603252	13603253	A	T	26	GENIC	homozygous	111088002
2	13603562	13603563	A	G	27	GENIC	homozygous	111088004
2	13603839	13603840	C	T	26	GENIC	homozygous	109610062
2	13603941	13603942	A	T	30	GENIC	homozygous	109610063
2	13604440	13604441	A	G	28	GENIC	homozygous	109610065
2	13605150	13605151	A	G	19	GENIC	homozygous	109610070
2	13605329	13605330	A	G	18	GENIC	homozygous	109610071
2	13605383	13605384	A	G	20	GENIC	homozygous	111088006
2	13607019	13607020	A	G	18	GENIC	homozygous	111088008
2	13608589	13608590	G	A	16	GENIC	homozygous	111088010
2	13609130	13609131	C	G	21	GENIC	homozygous	109610078
2	13609230	13609231	G	T	23	GENIC	homozygous	109610079
2	13611982	13611983	T	C	15	GENIC	homozygous	111088015
2	13612939	13612940	T	C	36	GENIC	homozygous	109610087
2	13613495	13613496	T	C	34	GENIC	homozygous	109610090
2	13613647	13613648	T	C	39	GENIC	homozygous	109610091