chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	38510091	38510092	A	G	68	GENIC	homozygous	115609615
12	38510867	38510868	C	T	54	GENIC	homozygous	115609617
12	38511525	38511526	A	G	56	GENIC	homozygous	115609619
12	38512031	38512032	A	G	14	GENIC	homozygous	115609621
12	38512439	38512440	G	A	39	GENIC	possibly homozygous	115609623
12	38512960	38512961	C	T	78	GENIC	homozygous	115609625
12	38513676	38513677	G	A	60	GENIC	homozygous	115609627
12	38514153	38514154	A	C	69	GENIC	homozygous	115609629
12	38514545	38514546	C	T	56	GENIC	homozygous	115609631
12	38515162	38515163	C	T	73	GENIC	possibly homozygous	115609633
12	38515621	38515622	T	C	56	GENIC	homozygous	115609635
12	38517402	38517403	A	G	28	GENIC	homozygous	115609637
12	38517775	38517776	T	A	10	GENIC	homozygous	115609639
12	38519212	38519213	G	A	24	GENIC	homozygous	115609641
12	38519590	38519591	T	A	51	GENIC	homozygous	115609643
12	38519961	38519962	T	C	21	GENIC	homozygous	115609645
12	38520230	38520231	T	C	62	GENIC	homozygous	115609647
12	38522417	38522418	T	C	37	GENIC	homozygous	115323141
12	38522562	38522563	A	C	54	GENIC	homozygous	115323143
12	38523010	38523011	C	T	35	GENIC	homozygous	115323145
12	38523351	38523352	T	C	31	GENIC	homozygous	115609649
12	38524551	38524552	A	G	84	GENIC	homozygous	115609651