chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	3125189	3125190	C	T	13	GENIC	heterozygous	53768174
7	3125189	3125190	C	CCT	11	GENIC	homozygous	53768176
7	3125341	3125342	G	A	31	GENIC	homozygous	53768178
7	3125872	3125876	GTGT	----	8	GENIC	heterozygous	53768179
7	3125874	3125876	GT	--	8	GENIC	heterozygous	53768181
7	3125911	3125912	T	C	33	GENIC	possibly homozygous	53768183
7	3125921	3125922	T	C	36	GENIC	possibly homozygous	53768185
7	3127415	3127440	CAGATCGTCTAGGATGGGAGCTACA	-------------------------	7	GENIC	homozygous	53768187
7	3128151	3128152	A	ACACAGGGAGATCCCTGGGCT	19	GENIC	homozygous	53768189
7	3128155	3128156	T	A	34	GENIC	heterozygous	53768191
7	3128656	3128657	C	G	45	GENIC	homozygous	53768193
7	3129301	3129303	GG	--	5	GENIC	heterozygous	53768195
7	3131429	3131430	C	T	53	GENIC	homozygous	53768199