chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	2989480	2989481	A	G	59	GENIC	possibly homozygous	115546245
7	2990404	2990405	T	C	43	GENIC	homozygous	115977356
7	2991711	2991712	C	G	45	GENIC	homozygous	116268512
7	2992081	2992082	G	A	33	GENIC	homozygous	115546247
7	2994781	2994782	T	C	33	GENIC	homozygous	115546253
7	2995780	2995781	C	T	53	GENIC	homozygous	116268513
7	2997063	2997064	G	A	39	GENIC	homozygous	115546255
7	2997665	2997666	A	G	21	GENIC	homozygous	115546261
7	2999727	2999728	C	T	31	GENIC	homozygous	116268514
7	3001268	3001269	A	G	35	GENIC	homozygous	115546265
7	3002257	3002258	C	G	33	GENIC	homozygous	115546273
7	3002874	3002875	A	G	46	GENIC	possibly homozygous	115546275
7	3004165	3004166	G	A	34	GENIC	homozygous	115546283
7	3004452	3004453	G	C	32	GENIC	homozygous	115546285
7	3006113	3006114	C	T	34	GENIC	homozygous	115546289
7	3006556	3006557	C	T	38	GENIC	homozygous	115546291
7	3007403	3007404	T	C	22	GENIC	homozygous	115546293
7	3008439	3008440	C	T	39	GENIC	homozygous	116268515
7	3008925	3008926	A	G	24	GENIC	homozygous	115546295
7	3008928	3008929	T	A	25	GENIC	homozygous	115546297
7	3009077	3009078	C	G	31	GENIC	homozygous	116268516
7	3009168	3009169	C	A	31	GENIC	homozygous	116268517
7	3009302	3009303	G	A	41	GENIC	possibly homozygous	116268518
7	3010008	3010009	T	A	31	GENIC	homozygous	115546301
7	3010467	3010468	A	G	41	GENIC	homozygous	115546305