chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	4108494	4108495	C	T	54	GENIC	homozygous	119382111
17	4108567	4108568	C	A	56	GENIC	homozygous	111154842
17	4108589	4108590	G	T	54	GENIC	possibly homozygous	119382113
17	4108679	4108680	C	T	39	GENIC	homozygous	111154844
17	4108683	4108684	T	G	39	GENIC	homozygous	111154846
17	4108733	4108734	C	T	35	GENIC	homozygous	111154848
17	4108849	4108850	T	C	50	GENIC	homozygous	111154852
17	4109002	4109003	T	C	47	GENIC	homozygous	111444490
17	4109332	4109333	A	G	33	GENIC	homozygous	119323865
17	4109334	4109335	T	C	34	GENIC	homozygous	119323866
17	4109508	4109509	T	G	50	GENIC	homozygous	119382115
17	4109526	4109527	A	G	50	GENIC	homozygous	111154856
17	4109586	4109587	A	G	56	GENIC	homozygous	111444493
17	4109606	4109607	A	G	51	GENIC	homozygous	111154858
17	4109724	4109725	T	C	30	GENIC	homozygous	119382117
17	4109798	4109799	A	G	50	GENIC	homozygous	119382119
17	4109857	4109858	G	C	45	GENIC	homozygous	119382121
17	4110093	4110094	G	A	38	GENIC	homozygous	119382123
17	4110113	4110114	T	A	40	GENIC	homozygous	119382125
17	4110330	4110331	C	T	28	GENIC	homozygous	119382127