chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	11254328	11254329	G	C	45	GENIC	possibly homozygous	115580398
12	11254525	11254526	C	T	62	GENIC	homozygous	115580400
12	11255856	11255857	G	A	56	GENIC	homozygous	115580402
12	11257116	11257117	A	C	45	GENIC	homozygous	115254942
12	11257300	11257301	G	A	40	GENIC	homozygous	115580404
12	11257550	11257551	A	G	30	GENIC	homozygous	115254946
12	11257711	11257712	C	T	53	GENIC	homozygous	115580406
12	11260950	11260951	A	G	50	GENIC	homozygous	115437342
12	11261271	11261272	A	T	46	GENIC	possibly homozygous	115580408
12	11261485	11261486	G	A	54	GENIC	possibly homozygous	115437343
12	11261836	11261837	G	A	48	GENIC	homozygous	115437344
12	11263127	11263128	A	T	39	GENIC	homozygous	115521329
12	11263208	11263209	C	T	52	GENIC	homozygous	115580412
12	11263795	11263796	T	G	53	GENIC	possibly homozygous	115254970
12	11264462	11264463	A	C	71	GENIC	homozygous	115580414
12	11265052	11265053	C	A	53	GENIC	homozygous	115254980
12	11265347	11265348	A	G	23	GENIC	homozygous	115254984