chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	37307810	37307811	C	T	56	GENIC	homozygous	142063886
8	37308280	37308281	G	C	61	GENIC	homozygous	142063887
8	37308419	37308420	T	C	67	GENIC	homozygous	142063888
8	37308432	37308433	C	T	59	GENIC	homozygous	142063889
8	37308964	37308965	T	C	49	GENIC	homozygous	142063890
8	37309367	37309376	AGACCTTTC		41	GENIC	homozygous	142022411
8	37310705	37310706	C	T	47	GENIC	homozygous	142063891
8	37311465	37311561	AGTATAAACATTTTTTTTTTCTTTTCTTTTTTTCGGAGCTGGGGACTGAACCCAGGGCCTTGCGCTTCCTAGGTAAGCGCTCTACCACTGAGCTAA		46	GENIC	homozygous	142022412
8	37312982	37313009	ATATGGCCCTTAAATGAAATGACTGAA		33	GENIC	homozygous	142022413
8	37314858	37314859	A	G	51	GENIC	homozygous	142063892
8	37315952	37315953	A	C	72	GENIC	homozygous	142063893
8	37316792	37316794	AC		38	GENIC	homozygous	142022414
8	37316830	37316831	G	A	41	GENIC	homozygous	142063894
8	37317038	37317039	T		36	GENIC	homozygous	142022415
8	37317086	37317087	A	G	44	GENIC	homozygous	142063895
8	37317190	37317193	TTT		32	GENIC	homozygous	142022416
8	37317301	37317302	C	T	35	GENIC	possibly homozygous	142063897
8	37316353	37316354	G		23	GENIC	heterozygous	403234109
8	37316353	37316354	G	C	23	GENIC	heterozygous	403234110
8	37317285	37317286	T		31	GENIC	possibly homozygous	403234113
8	37317285	37317286	T	C	31	GENIC	heterozygous	403234114
8	37317297	37317298	C	T	34	GENIC	possibly homozygous	142063896
8	37318176	37318177	T	A	46	GENIC	homozygous	142063899
8	37317975	37317976	C	T	51	GENIC	homozygous	142063898