chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	52855757	52855758	C	T	19	GENIC	homozygous	114346249
13	52855821	52855822	T	A	22	GENIC	homozygous	114346251
13	52855860	52855861	G	A	31	GENIC	homozygous	114346253
13	52855989	52855990	T	A	42	GENIC	homozygous	114346255
13	52856338	52856339	T	G	65	GENIC	homozygous	114346257
13	52856402	52856403	G	A	66	GENIC	homozygous	114346259
13	52856539	52856540	C	T	57	GENIC	homozygous	114346261
13	52856656	52856657	T	C	45	GENIC	homozygous	114346263
13	52856662	52856663	A	G	44	GENIC	homozygous	114346265
13	52858050	52858051	G	A	36	GENIC	homozygous	114346267
13	52858622	52858623	C	T	49	GENIC	homozygous	114346269
13	52859268	52859269	T	C	42	GENIC	homozygous	114346271
13	52859996	52859997	G	A	36	GENIC	homozygous	114346273
13	52860440	52860441	G	A	43	GENIC	homozygous	114346275
13	52860530	52860531	T	C	21	GENIC	homozygous	114346277
13	52861933	52861934	T	C	42	GENIC	homozygous	114346279
13	52862098	52862099	T	C	35	GENIC	homozygous	114346281
13	52862346	52862347	C	T	24	GENIC	homozygous	114346283
13	52862813	52862814	A	G	38	GENIC	homozygous	114346285
13	52863187	52863188	G	A	45	GENIC	homozygous	114346287
13	52867305	52867306	A	G	37	GENIC	homozygous	114346289
13	52869240	52869241	T	G	41	GENIC	homozygous	114346291
13	52870722	52870723	A	G	50	GENIC	homozygous	114346293
13	52870885	52870886	C	A	32	GENIC	homozygous	114346295