chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	18602410	18602411	G	C	34	GENIC	homozygous	116503473
10	18603551	18603552	T	C	47	GENIC	homozygous	116503475
10	18603707	18603708	A	G	47	GENIC	homozygous	116503477
10	18603709	18603710	T	C	46	GENIC	homozygous	116503479
10	18603785	18603786	G	A	34	GENIC	homozygous	116503481
10	18603876	18603877	G	A	44	GENIC	homozygous	116503483
10	18604342	18604343	T	C	40	GENIC	homozygous	116503485
10	18604442	18604443	G	T	33	GENIC	possibly homozygous	116503487
10	18605073	18605074	G	A	48	GENIC	homozygous	116503489
10	18605919	18605920	G	A	36	GENIC	homozygous	116503491
10	18606652	18606653	C	T	36	GENIC	homozygous	116503493
10	18607659	18607660	C	T	40	GENIC	homozygous	116503495
10	18607903	18607904	A	G	35	GENIC	homozygous	116503497
10	18608206	18608207	A	C	24	GENIC	homozygous	116503499
10	18608557	18608558	A	G	28	GENIC	homozygous	116503501
10	18609171	18609172	T	C	50	GENIC	homozygous	116503503