chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	199844870	199844871	G	T	26	GENIC	homozygous	108502200
1	199844871	199844872	G	C	26	GENIC	homozygous	108502202
1	199844879	199844880	G	A	28	GENIC	homozygous	108502204
1	199844898	199844899	G	T	27	GENIC	homozygous	108502206
1	199844913	199844914	G		26	GENIC	homozygous	127472996
1	199844915	199844916	G	A	26	GENIC	homozygous	121160432
1	199844917	199844924	GGGGGTG		26	GENIC	homozygous	127472997
1	199844925	199844925		TTCATAT	25	GENIC	homozygous	127472998
1	199844950	199844951	G		26	GENIC	homozygous	127472999
1	199844954	199844954		C	26	GENIC	homozygous	127473000
1	199844966	199844967	G		26	GENIC	homozygous	127473001
1	199844969	199844970	G	C	26	GENIC	homozygous	108502208
1	199844971	199844972	G	T	25	GENIC	homozygous	108502210
1	199844973	199844974	G	T	23	GENIC	homozygous	108502212
1	199844993	199844994	G	T	30	GENIC	homozygous	108502214
1	199844995	199844996	G	C	31	GENIC	homozygous	108502216
1	199845034	199845035	G	T	43	GENIC	homozygous	108502218
1	199845040	199845041	C		42	GENIC	homozygous	127473002
1	199845046	199845046		T	41	GENIC	homozygous	127473003
1	199845077	199845078	A	G	40	GENIC	homozygous	120892471
1	199845047	199845048	G	T	41	GENIC	homozygous	120912619
1	199845058	199845059	G	T	43	GENIC	homozygous	120475419
1	199845059	199845060	T	G	43	GENIC	homozygous	120475420
1	199845061	199845062	T	C	41	GENIC	homozygous	120475421
1	199845078	199845079	G	A	41	GENIC	homozygous	120475422
1	199859405	199859406	G		18	GENIC	homozygous	127473005
1	199859411	199859412	G		16	GENIC	homozygous	127473006
1	199859415	199859416	G		15	GENIC	homozygous	127473007
1	199859417	199859418	G	A	14	GENIC	homozygous	121160446
1	199859420	199859422	GG		12	GENIC	homozygous	127473008
1	199859426	199859427	G	A	10	GENIC	homozygous	121160448
1	199859432	199859435	GAG		8	GENIC	homozygous	127473009
1	199859438	199859441	GAG		8	GENIC	homozygous	127473010
1	199859455	199859457	CG		3	GENIC	homozygous	127473012