chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	27466172	27466173	C	T	9	GENIC	homozygous	114304193
13	27466261	27466262	G	A	24	GENIC	homozygous	114304194
13	27467546	27467547	T	C	14	GENIC	homozygous	114304195
13	27467816	27467817	C	G	16	GENIC	homozygous	114304196
13	27468539	27468540	C	T	18	GENIC	homozygous	114304197
13	27472029	27472030	C	T	22	GENIC	homozygous	114304200
13	27472832	27472833	A	T	17	GENIC	homozygous	114304201
13	27473003	27473004	A	C	16	GENIC	homozygous	114304202
13	27474495	27474496	G	A	17	GENIC	homozygous	114304203
13	27475802	27475803	A	G	13	GENIC	homozygous	114304204
13	27476468	27476469	T	C	35	GENIC	homozygous	114304205
13	27477341	27477342	C	T	35	GENIC	homozygous	114304206
13	27477729	27477730	G	A	21	GENIC	homozygous	114304207
13	27477864	27477865	A	T	20	GENIC	homozygous	114304208
13	27478117	27478118	T	C	12	GENIC	homozygous	114304209
13	27478858	27478859	C	T	20	GENIC	homozygous	114304210
13	27480437	27480438	T	A	21	GENIC	homozygous	114304211
13	27480494	27480495	C	A	21	GENIC	homozygous	114304212
13	27481100	27481101	G	A	23	GENIC	homozygous	114304213
13	27482130	27482131	G	A	8	GENIC	homozygous	114304214
13	27482783	27482784	T	C	16	GENIC	homozygous	114517705
13	27482900	27482901	A	G	19	GENIC	homozygous	114517707
13	27483205	27483206	G	A	20	GENIC	homozygous	114517711
13	27483431	27483432	T	C	22	GENIC	homozygous	114304215
13	27483296	27483297	C	T	22	GENIC	homozygous	114815430