chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	80159393	80159394	T	C	37	GENIC	homozygous	115127584
6	80159885	80159886	C	T	30	GENIC	homozygous	115262900
6	80159900	80159901	C	T	28	GENIC	homozygous	115262902
6	80159901	80159902	C	T	28	GENIC	homozygous	115127585
6	80160461	80160462	T	C	29	GENIC	homozygous	115127586
6	80160719	80160720	A	C	28	GENIC	homozygous	115127587
6	80160809	80160810	C	T	27	GENIC	homozygous	115127588
6	80160856	80160857	G	A	17	GENIC	homozygous	115262904
6	80161053	80161054	A	G	35	GENIC	homozygous	115127590
6	80161084	80161085	T	C	31	GENIC	homozygous	115127591
6	80161093	80161094	G	C	31	GENIC	homozygous	115127592
6	80161139	80161140	C	T	18	GENIC	possibly homozygous	115262906
6	80161557	80161558	G	A	21	GENIC	homozygous	115262908
6	80161910	80161911	T	C	17	GENIC	homozygous	115127593
6	80161963	80161964	A	T	18	GENIC	homozygous	115127594
6	80162591	80162592	G	T	20	GENIC	possibly homozygous	115127595
6	80163394	80163395	G	A	11	GENIC	homozygous	115262910
6	80163456	80163457	T	C	12	GENIC	homozygous	115127598
6	80163847	80163848	A	G	17	GENIC	homozygous	115127599
6	80163976	80163977	G	A	24	GENIC	homozygous	115127600
6	80164278	80164279	G	A	17	GENIC	homozygous	115262912
6	80164522	80164523	C	A	15	GENIC	homozygous	115127601
6	80165027	80165028	A	G	21	GENIC	homozygous	115127602
6	80165160	80165161	T	A	13	GENIC	homozygous	115127603
6	80165253	80165254	G	A	20	GENIC	homozygous	115127604
6	80165276	80165277	C	T	25	GENIC	homozygous	115127605
6	80165538	80165539	A	G	28	GENIC	homozygous	115127606
6	80165945	80165946	A	G	35	GENIC	homozygous	115127607