chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	97940957	97940958	T	G	22	GENIC	heterozygous	130684030
10	97940983	97940984	C		26	GENIC	homozygous	128850840
10	97940989	97940990	A		26	GENIC	homozygous	128850841
10	97940993	97940994	C		27	GENIC	homozygous	128850842
10	97940998	97940999	C		27	GENIC	homozygous	128850843
10	97941002	97941003	A		29	GENIC	homozygous	128850844
10	97941004	97941006	CT		29	GENIC	homozygous	128850845
10	97941077	97941077		C	47	GENIC	homozygous	128850846
10	97941160	97941160		C	46	GENIC	homozygous	128850847
10	97941197	97941197		C	42	GENIC	homozygous	128850848
10	97941226	97941227	C		39	GENIC	homozygous	128850849
10	97941231	97941232	C		40	GENIC	homozygous	128850850
10	97941255	97941256	C		31	GENIC	homozygous	128850851
10	97941311	97941311		CGCC	29	GENIC	homozygous	128850852
10	97941317	97941318	A		28	GENIC	homozygous	128850853
10	97941418	97941419	C		43	GENIC	homozygous	128850854
10	97941438	97941438		G	51	GENIC	homozygous	128850855
10	97941444	97941444		CC	51	GENIC	homozygous	128850856
10	97941460	97941461	C		56	GENIC	homozygous	128850857
10	97940994	97940995	C	T	27	GENIC	homozygous	116907048
10	97947166	97947167	G	T	10	GENIC	homozygous	129974028
10	97947168	97947169	A	C	9	GENIC	homozygous	129974029
10	97958216	97958216		TG	59	GENIC	possibly homozygous	131709694