chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	80109556	80109557	T	C	12	GENIC	homozygous	115127496
6	80109772	80109773	A	G	11	GENIC	homozygous	115262826
6	80110250	80110251	A	G	34	GENIC	homozygous	115127499
6	80110357	80110358	G	A	22	GENIC	homozygous	115262828
6	80110971	80110972	G	A	23	GENIC	homozygous	115127501
6	80111583	80111584	G	A	11	GENIC	homozygous	115262830
6	80112678	80112679	T	G	19	GENIC	homozygous	115262832
6	80113039	80113040	A	G	31	GENIC	homozygous	115262834
6	80114052	80114053	T	C	30	GENIC	homozygous	115262836
6	80114639	80114640	T	C	20	GENIC	homozygous	115262838
6	80114671	80114672	T	C	28	GENIC	homozygous	115127503
6	80116346	80116347	G	C	32	GENIC	homozygous	115127504
6	80117117	80117118	T	C	18	GENIC	homozygous	115262840
6	80117383	80117384	T	C	34	GENIC	homozygous	115127507
6	80118299	80118300	T	C	21	GENIC	homozygous	115127509
6	80120465	80120466	C	T	14	GENIC	homozygous	115262842
6	80120610	80120611	G	A	6	GENIC	homozygous	115262844
6	80120844	80120845	T	C	19	GENIC	homozygous	114869611
6	80121580	80121581	C	T	30	GENIC	homozygous	115262846
6	80121593	80121594	C	A	34	GENIC	homozygous	115262848
6	80121874	80121875	G	A	30	GENIC	homozygous	115127516
6	80121878	80121879	A	T	30	GENIC	homozygous	115262850