chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	27450910	27450911	A	G	29	GENIC	homozygous	114304165
13	27452778	27452779	T	C	24	GENIC	homozygous	114304166
13	27453775	27453776	C	T	33	GENIC	homozygous	114304167
13	27454524	27454525	T	C	38	GENIC	homozygous	114304168
13	27454989	27454990	G	T	26	GENIC	homozygous	114304169
13	27457872	27457873	G	C	21	GENIC	homozygous	114304170
13	27457999	27458000	A	C	29	GENIC	homozygous	114304171
13	27458243	27458244	C	A	24	GENIC	homozygous	114304172
13	27458736	27458737	G	T	38	GENIC	homozygous	114304173
13	27458737	27458738	G	A	38	GENIC	homozygous	114304174
13	27458807	27458808	T	A	30	GENIC	homozygous	114304175
13	27460068	27460069	T	C	35	GENIC	homozygous	114304176
13	27460183	27460184	C	T	39	GENIC	homozygous	114304177
13	27461126	27461127	C	T	40	GENIC	homozygous	114304178
13	27461288	27461289	C	G	42	GENIC	homozygous	114304179
13	27461326	27461327	A	G	26	GENIC	possibly homozygous	114304180
13	27461392	27461393	A	G	28	GENIC	homozygous	114304181
13	27461651	27461652	T	A	20	GENIC	homozygous	114304182
13	27462756	27462757	C	T	29	GENIC	homozygous	114304183
13	27460748	27460749	T	C	19	GENIC	homozygous	114608752