chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	47384235	47384236	C	T	7	GENIC	homozygous	111057281
17	47384248	47384249	C	T	7	GENIC	homozygous	111057282
17	47384251	47384252	T	A	8	GENIC	homozygous	111057283
17	47384684	47384685	C	T	25	GENIC	homozygous	111057284
17	47384842	47384843	C	T	18	GENIC	possibly homozygous	111057285
17	47384970	47384971	T	C	29	GENIC	homozygous	111057286
17	47385167	47385168	T	C	8	GENIC	homozygous	111057287
17	47385405	47385406	G	T	6	GENIC	homozygous	111057288
17	47385756	47385757	C	T	22	GENIC	homozygous	111057290
17	47385976	47385977	G	A	12	GENIC	homozygous	111057291
17	47386063	47386064	G	A	16	GENIC	homozygous	111057292
17	47386522	47386523	T	G	14	GENIC	homozygous	111057295
17	47387707	47387708	T	A	4	GENIC	homozygous	111057296
17	47387966	47387967	G	A	20	GENIC	homozygous	111057297
17	47388000	47388001	C	T	12	GENIC	homozygous	111057298
17	47388060	47388061	T	C	16	GENIC	homozygous	111057299
17	47388068	47388069	A	G	14	GENIC	homozygous	111057300
17	47388179	47388180	T	C	7	GENIC	homozygous	111057301
17	47388314	47388315	G	T	7	GENIC	homozygous	111057302
17	47388730	47388731	T	A	20	GENIC	homozygous	111057303
17	47389254	47389255	T	A	4	GENIC	homozygous	111426904
17	47387355	47387356	T	G	8	GENIC	homozygous	119342900
17	47389225	47389226	C	T	7	GENIC	homozygous	111245276
17	47389784	47389785	G	C	12	GENIC	homozygous	111057306
17	47391032	47391033	C	T	16	GENIC	homozygous	111057307
17	47391189	47391190	A	T	8	GENIC	homozygous	111057308
17	47391427	47391428	G	C	6	GENIC	homozygous	111057309
17	47391156	47391157	G	A	7	GENIC	homozygous	111348929
17	47393504	47393505	A	G	14	GENIC	homozygous	111057310
17	47393765	47393766	G	T	18	GENIC	homozygous	111057311