chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	41059676	41059677	G	T	37	GENIC	homozygous	114768880
6	41060008	41060009	C	T	40	GENIC	homozygous	114768882
6	41060405	41060406	T	C	32	GENIC	homozygous	114768884
6	41060936	41060937	C	T	42	GENIC	homozygous	114768886
6	41061525	41061526	A	G	35	GENIC	homozygous	114768888
6	41061680	41061681	A	G	45	GENIC	homozygous	114768890
6	41062607	41062608	C	A	33	GENIC	homozygous	114768892
6	41063044	41063045	G	A	56	GENIC	homozygous	114768894
6	41063781	41063782	G	T	33	GENIC	homozygous	114768896
6	41063806	41063807	T	C	30	GENIC	homozygous	114768898
6	41064148	41064149	A	G	51	GENIC	homozygous	114768900
6	41064289	41064290	C	G	35	GENIC	homozygous	114768902
6	41064899	41064900	G	C	28	GENIC	homozygous	114768904
6	41066273	41066274	A	G	22	GENIC	heterozygous	114768906
6	41066892	41066893	A	G	38	GENIC	possibly homozygous	114768908
6	41067387	41067388	T	C	26	GENIC	heterozygous	114768910
6	41068492	41068493	A	G	39	GENIC	homozygous	114768912
6	41068506	41068507	A	G	40	GENIC	homozygous	114768914
6	41068514	41068515	C	T	36	GENIC	homozygous	114768916
6	41068520	41068521	C	T	30	GENIC	homozygous	114768918
6	41068532	41068533	C	T	30	GENIC	homozygous	114768920
6	41068560	41068561	A	G	21	GENIC	homozygous	114768922
6	41068564	41068565	C	G	21	GENIC	homozygous	115056940
6	41068565	41068566	C	T	21	GENIC	possibly homozygous	115056942
6	41068566	41068567	A	T	21	GENIC	homozygous	115056944
6	41069077	41069078	G	C	38	GENIC	homozygous	114768926
6	41069257	41069258	G	A	39	GENIC	homozygous	114768928
6	41066250	41066251	A	G	14	GENIC	possibly homozygous	115244341