chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	52855757	52855758	C	T	9	GENIC	homozygous	114346249
13	52855821	52855822	T	A	13	GENIC	homozygous	114346251
13	52855860	52855861	G	A	21	GENIC	homozygous	114346253
13	52855989	52855990	T	A	15	GENIC	homozygous	114346255
13	52856338	52856339	T	G	30	GENIC	homozygous	114346257
13	52856402	52856403	G	A	29	GENIC	homozygous	114346259
13	52856539	52856540	C	T	25	GENIC	homozygous	114346261
13	52856656	52856657	T	C	25	GENIC	homozygous	114346263
13	52856662	52856663	A	G	27	GENIC	homozygous	114346265
13	52858050	52858051	G	A	18	GENIC	homozygous	114346267
13	52858622	52858623	C	T	34	GENIC	homozygous	114346269
13	52859268	52859269	T	C	37	GENIC	homozygous	114346271
13	52859996	52859997	G	A	32	GENIC	homozygous	114346273
13	52860440	52860441	G	A	29	GENIC	homozygous	114346275
13	52860530	52860531	T	C	6	GENIC	homozygous	114346277
13	52861933	52861934	T	C	26	GENIC	homozygous	114346279
13	52862098	52862099	T	C	33	GENIC	homozygous	114346281
13	52862346	52862347	C	T	18	GENIC	homozygous	114346283
13	52862813	52862814	A	G	35	GENIC	homozygous	114346285
13	52863187	52863188	G	A	46	GENIC	homozygous	114346287
13	52867305	52867306	A	G	24	GENIC	homozygous	114346289
13	52869240	52869241	T	G	43	GENIC	homozygous	114346291
13	52870722	52870723	A	G	46	GENIC	homozygous	114346293