chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	107186524	107186528	AAAG		29	GENIC	homozygous	128503329
7	107186529	107186529		TTC	29	GENIC	homozygous	128503330
7	107186530	107186531	A	T	29	GENIC	homozygous	118258153
7	107186530	107186530		T	29	GENIC	homozygous	128503331
7	107206195	107206196	T		12	GENIC	homozygous	128503332
7	107206218	107206219	G		12	GENIC	homozygous	128503333
7	107206232	107206233	T		13	GENIC	homozygous	128503334
7	107206252	107206253	C		13	GENIC	homozygous	128503335
7	107206342	107206343	T	G	8	GENIC	homozygous	115807345
7	107206179	107206180	G		13	GENIC	homozygous	129938772
7	107216392	107216392		C	19	GENIC	homozygous	128503337
7	107216401	107216403	TT		16	GENIC	homozygous	128503338
7	107216447	107216448	T		21	GENIC	homozygous	128503339
7	107216486	107216487	A		20	GENIC	homozygous	128503340
7	107216498	107216498		AT	16	GENIC	homozygous	128503341
7	107216502	107216503	A		16	GENIC	homozygous	128503342
7	107216506	107216507	A		16	GENIC	homozygous	128503343
7	107216549	107216550	C	A	16	GENIC	homozygous	118258155
7	107216550	107216551	A	C	17	GENIC	homozygous	118320210
7	107216584	107216585	G	A	30	GENIC	homozygous	115807369
7	107216630	107216631	G		22	GENIC	homozygous	128503344
7	107216653	107216654	T		20	GENIC	homozygous	128503345
7	107216681	107216681		A	18	GENIC	homozygous	128503346