chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	42092696	42092697	T	G	29	GENIC	homozygous	114773188
6	42093622	42093623	A	T	30	GENIC	homozygous	115206603
6	42095047	42095048	A	C	17	GENIC	homozygous	114773202
6	42095889	42095890	G	A	26	GENIC	homozygous	115206604
6	42096578	42096579	T	C	31	GENIC	homozygous	115206605
6	42097012	42097013	G	A	46	GENIC	homozygous	115206606
6	42099674	42099675	A	G	16	GENIC	homozygous	114773240
6	42101145	42101146	C	A	22	GENIC	possibly homozygous	114773252
6	42102138	42102139	A	G	27	GENIC	homozygous	114773258
6	42102426	42102427	A	G	11	GENIC	possibly homozygous	114773262
6	42102429	42102430	C	T	12	GENIC	possibly homozygous	115206607
6	42102777	42102778	G	C	19	GENIC	heterozygous	115206608
6	42103561	42103562	C	T	13	GENIC	homozygous	115206609
6	42104022	42104023	T	G	4	GENIC	homozygous	115206610
6	42104023	42104024	C	A	3	GENIC	homozygous	115206611
6	42104076	42104077	T	C	10	GENIC	possibly homozygous	114773266
6	42104124	42104125	C	A	8	GENIC	homozygous	114773270
6	42105585	42105586	T	G	17	GENIC	heterozygous	115206612
6	42106459	42106460	G	T	23	GENIC	homozygous	115206613
6	42106673	42106674	C	T	22	GENIC	homozygous	115206614
6	42106819	42106820	C	G	33	GENIC	homozygous	115206615
6	42107920	42107921	A	G	24	GENIC	homozygous	114773274