chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	31642526	31642527	G	A	64	GENIC	homozygous	116351604
11	31644188	31644189	T		41	GENIC	homozygous	130778849
11	31646225	31646226	T	C	50	GENIC	homozygous	115812274
11	31644838	31644839	G	A	51	GENIC	homozygous	131717930
11	31644839	31644840	G	A	51	GENIC	homozygous	131717931
11	31646010	31646011	T	G	65	GENIC	possibly homozygous	115812272
11	31646638	31646639	C	T	67	GENIC	homozygous	115812276
11	31649507	31649508	A	T	2	GENIC	homozygous	118179936
11	31651547	31651548	T	A	47	GENIC	homozygous	115812280
11	31650892	31650892		A	37	GENIC	heterozygous	130399819
11	31652035	31652036	C	T	39	GENIC	homozygous	116351605
11	31652476	31652477	G	A	46	GENIC	homozygous	115812282
11	31653461	31653462	T	A	46	GENIC	homozygous	115812284
11	31654234	31654235	C	T	50	GENIC	homozygous	116351606
11	31654571	31654572	A	T	55	GENIC	homozygous	115812288
11	31655615	31655616	T	G	60	GENIC	homozygous	115812296
11	31656484	31656485	T	C	74	GENIC	possibly homozygous	131717932
11	31656642	31656643	A	C	55	GENIC	possibly homozygous	118141590
11	31658065	31658066	G	A	15	GENIC	homozygous	131717933
11	31658089	31658090	G	C	19	GENIC	homozygous	118141597
11	31658443	31658444	A	G	59	GENIC	homozygous	115812300
11	31658750	31658751	T	C	33	GENIC	homozygous	116351607
11	31660001	31660002	T	C	52	GENIC	possibly homozygous	115812302
11	31660321	31660322	G	A	53	GENIC	homozygous	116351608
11	31663290	31663291	T	C	50	GENIC	homozygous	116351609
11	31652817	31652837	CGCGAGTGGGTATGTGCGCG		34	GENIC	homozygous	131715596
11	31653610	31653611	G		57	GENIC	homozygous	131715597
11	31658766	31658767	C		34	GENIC	homozygous	131715598