chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	17538167	17538168	A	G	59	GENIC	homozygous	115766465
11	17540137	17540138	T	C	31	GENIC	homozygous	115766471
11	17544441	17544442	A	C	48	GENIC	homozygous	115766473
11	17545834	17545835	T	C	43	GENIC	homozygous	115766475
11	17545874	17545875	C	T	51	GENIC	homozygous	115766477
11	17546059	17546060	C	T	43	GENIC	possibly homozygous	116239318
11	17546111	17546112	T	G	47	GENIC	homozygous	116239319
11	17547723	17547724	A	C	37	GENIC	homozygous	115766483
11	17548688	17548689	A	G	57	GENIC	homozygous	116239320
11	17548724	17548725	T	A	46	GENIC	homozygous	115766485
11	17550912	17550913	T	C	36	GENIC	homozygous	115766487
11	17552331	17552332	T	A	47	GENIC	possibly homozygous	116239321
11	17553837	17553838	C	T	37	GENIC	homozygous	116239322
11	17554560	17554561	C	T	29	GENIC	homozygous	116239323
11	17555921	17555922	C	A	50	GENIC	homozygous	116239324
11	17556823	17556824	T	C	45	GENIC	homozygous	116027941
11	17557121	17557122	C	T	23	GENIC	homozygous	116239325
11	17557425	17557426	T	C	44	GENIC	homozygous	115766499
11	17557853	17557854	G	A	47	GENIC	homozygous	116239326
11	17560149	17560150	G	C	51	GENIC	homozygous	116239327
11	17554256	17554257	A	C	38	GENIC	homozygous	115949901
11	17552864	17552865	C	A	26	GENIC	homozygous	115949900