chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	41059676	41059677	G	T	16	GENIC	homozygous	114768880
6	41060008	41060009	C	T	14	GENIC	homozygous	114768882
6	41060887	41060888	G	A	25	GENIC	homozygous	115499310
6	41060936	41060937	C	T	22	GENIC	homozygous	114768886
6	41061680	41061681	A	G	14	GENIC	homozygous	114768890
6	41062607	41062608	C	A	24	GENIC	homozygous	114768892
6	41063044	41063045	G	A	21	GENIC	homozygous	114768894
6	41063781	41063782	G	T	13	GENIC	homozygous	114768896
6	41063890	41063891	T	G	21	GENIC	homozygous	115499312
6	41064148	41064149	A	G	34	GENIC	homozygous	114768900
6	41064899	41064900	G	C	17	GENIC	homozygous	114768904
6	41065666	41065667	A	T	11	GENIC	homozygous	115205740
6	41065684	41065685	G	A	9	GENIC	homozygous	115205741
6	41066484	41066485	A	G	25	GENIC	homozygous	115205742
6	41066720	41066721	G	A	23	GENIC	homozygous	115205743
6	41066741	41066742	T	C	23	GENIC	homozygous	115205744
6	41066892	41066893	A	G	20	GENIC	homozygous	114768908
6	41068080	41068081	T	C	20	GENIC	homozygous	115205746
6	41068103	41068104	C	T	19	GENIC	homozygous	115205747