chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	54159673	54159676	CCC	---	35	GENIC	homozygous	49952162
13	54159914	54159915	T	-	54	GENIC	possibly homozygous	49952163
13	54163234	54163235	G	T	65	GENIC	homozygous	49952164
13	54163863	54163864	G	C	45	GENIC	homozygous	49952165
13	54165020	54165023	GTA	---	46	GENIC	homozygous	49952166
13	54166421	54166422	A	G	47	GENIC	homozygous	49952167
13	54166424	54166425	C	T	48	GENIC	homozygous	49952168
13	54166645	54166646	G	C	81	GENIC	homozygous	49952169
13	54167001	54167002	T	C	54	GENIC	homozygous	49952170
13	54167839	54167840	G	A	47	GENIC	homozygous	49952171
13	54168357	54168358	G	C	79	GENIC	homozygous	49952172
13	54168872	54168873	C	CAG	48	GENIC	homozygous	49952173
13	54168988	54168989	C	T	51	GENIC	homozygous	49952174
13	54169564	54169565	G	A	45	GENIC	homozygous	49952175
13	54170277	54170278	G	T	42	GENIC	homozygous	49952176
13	54170767	54170768	T	C	58	GENIC	homozygous	49952177
13	54171000	54171010	TGTGTGTGTG	----------	9	GENIC	possibly homozygous	49952178
13	54171032	54171033	T	C	32	GENIC	heterozygous	49952179
13	54171040	54171041	T	C	32	GENIC	possibly homozygous	49952180
13	54171229	54171230	C	G	30	GENIC	homozygous	49952181
13	54172495	54172496	A	G	54	GENIC	homozygous	49952182
13	54172825	54172826	C	T	54	GENIC	homozygous	49952183
13	54173045	54173046	T	C	60	GENIC	homozygous	49952184
13	54173690	54173691	A	G	54	GENIC	homozygous	49952185
13	54173947	54173948	C	CG	35	GENIC	homozygous	49952186
13	54174047	54174048	C	T	70	GENIC	possibly homozygous	49952187
13	54174986	54174990	TCCC	----	10	GENIC	possibly homozygous	49952188
13	54176407	54176408	A	G	42	GENIC	homozygous	49952189