chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	31569794	31569795	C		14	GENIC	homozygous	131464702
10	31569802	31569803	C		14	GENIC	homozygous	131464703
10	31569819	31569820	C		15	GENIC	homozygous	131464704
10	31569831	31569832	A		18	GENIC	homozygous	131464705
10	31569856	31569857	C		19	GENIC	homozygous	130681631
10	31569858	31569860	AC		19	GENIC	homozygous	130681632
10	31569879	31569884	CCATA		17	GENIC	homozygous	130681633
10	31569891	31569891		A	16	GENIC	homozygous	130681634
10	31569908	31569909	G		13	GENIC	homozygous	130681635
10	31569928	31569928		A	13	GENIC	homozygous	130681636
10	31569941	31569942	A		10	GENIC	homozygous	130681637
10	31569957	31569958	C		9	GENIC	homozygous	130681638
10	31569995	31569997	GG		35	GENIC	homozygous	128803629
10	31570004	31570005	G		36	GENIC	homozygous	128803630
10	31570034	31570035	T		34	GENIC	homozygous	128803631
10	31570045	31570046	C		35	GENIC	homozygous	128803632
10	31570051	31570052	A	T	35	GENIC	homozygous	116546862
10	31570053	31570054	C		35	GENIC	homozygous	128803633
10	31570125	31570125		C	32	GENIC	homozygous	128803634
10	31570138	31570139	A		36	GENIC	homozygous	128803635