chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	53584093	53584094	G	A	16	GENIC	homozygous	116887284
10	53584164	53584165	T	C	14	GENIC	homozygous	116887286
10	53584416	53584417	T	G	15	GENIC	homozygous	116887288
10	53584484	53584485	A	G	19	GENIC	homozygous	116887290
10	53584573	53584574	G	A	12	GENIC	homozygous	116887292
10	53586276	53586277	C	T	19	GENIC	homozygous	116887298
10	53586611	53586612	C	T	11	GENIC	homozygous	116887300
10	53587797	53587798	C	T	16	GENIC	homozygous	116887302
10	53588115	53588116	A	G	18	GENIC	homozygous	116887306
10	53588625	53588626	C	T	20	GENIC	homozygous	116887308
10	53589001	53589002	C	T	8	GENIC	homozygous	116887310
10	53589294	53589295	A	G	13	GENIC	homozygous	116887312
10	53589666	53589667	A	G	12	GENIC	homozygous	116887314
10	53589816	53589817	T	C	23	GENIC	homozygous	117078808
10	53590279	53590280	A	G	15	GENIC	homozygous	116887316
10	53591613	53591614	G	A	24	GENIC	homozygous	116887318
10	53592271	53592272	T	C	6	GENIC	heterozygous	116887320
10	53592754	53592755	C	T	13	GENIC	homozygous	116887322
10	53594286	53594287	T	C	4	GENIC	heterozygous	126431150
10	53594489	53594490	C	T	11	GENIC	homozygous	116887324
10	53595261	53595262	A	G	20	GENIC	homozygous	116887326
10	53595423	53595424	T	C	10	GENIC	homozygous	116887328
10	53595759	53595760	T	C	10	GENIC	homozygous	116887330