chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	36645463	36645464	C	T	38	GENIC	homozygous	116142793
7	36646270	36646271	T	C	18	GENIC	homozygous	115646997
7	36649886	36649887	A	G	30	GENIC	heterozygous	115647001
7	36650154	36650155	C	T	14	GENIC	possibly homozygous	116142795
7	36650548	36650549	T	C	39	GENIC	homozygous	115647006
7	36650698	36650699	A	G	29	GENIC	homozygous	115647007
7	36650824	36650825	A	G	19	GENIC	homozygous	116020807
7	36651136	36651137	A	T	18	GENIC	homozygous	116142797
7	36651931	36651932	C	T	29	GENIC	homozygous	116142799
7	36654588	36654589	A	G	17	GENIC	homozygous	115647010
7	36654790	36654791	C	T	16	GENIC	homozygous	116142801
7	36655517	36655518	C	T	26	GENIC	homozygous	116142803
7	36657423	36657424	C	A	37	GENIC	homozygous	116020811
7	36658508	36658509	G	A	30	GENIC	homozygous	115647015
7	36659406	36659407	C	T	29	GENIC	homozygous	115647016
7	36659660	36659661	G	A	29	GENIC	homozygous	116020813
7	36659773	36659774	A	G	28	GENIC	homozygous	116020815
7	36659828	36659829	G	A	32	GENIC	homozygous	116020819