chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	37307810	37307811	C	T	66	GENIC	homozygous	142063886
8	37308280	37308281	G	C	55	GENIC	homozygous	142063887
8	37308419	37308420	T	C	47	GENIC	homozygous	142063888
8	37308432	37308433	C	T	45	GENIC	homozygous	142063889
8	37308964	37308965	T	C	50	GENIC	homozygous	142063890
8	37309367	37309376	AGACCTTTC		49	GENIC	homozygous	142022411
8	37310705	37310706	C	T	38	GENIC	homozygous	142063891
8	37311465	37311561	AGTATAAACATTTTTTTTTTCTTTTCTTTTTTTCGGAGCTGGGGACTGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAA		33	GENIC	homozygous	142022412
8	37312982	37313009	ATATGGCCCTTAAATGAAATGACTGAA		45	GENIC	homozygous	142022413
8	37314858	37314859	A	G	51	GENIC	homozygous	142063892
8	37315952	37315953	A	C	64	GENIC	homozygous	142063893
8	37316792	37316794	AC		33	GENIC	homozygous	142022414
8	37316830	37316831	G	A	39	GENIC	homozygous	142063894
8	37317038	37317039	T		30	GENIC	homozygous	142022415
8	37317086	37317087	A	G	41	GENIC	homozygous	142063895
8	37317190	37317193	TTT		27	GENIC	homozygous	142022416
8	37317285	37317286	T	C	29	GENIC	heterozygous	403234114
8	37316353	37316354	G		15	GENIC	heterozygous	403234109
8	37316353	37316354	G	C	15	GENIC	heterozygous	403234110
8	37317285	37317286	T		29	GENIC	homozygous	403234113
8	37317297	37317298	C	T	30	GENIC	homozygous	142063896
8	37317301	37317302	C	T	32	GENIC	homozygous	142063897
8	37317975	37317976	C	T	55	GENIC	homozygous	142063898
8	37318176	37318177	T	A	49	GENIC	homozygous	142063899