chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	13346453	13346454	C	T	19	GENIC	homozygous	115362625
12	13348203	13348204	C	G	16	GENIC	homozygous	115260527
12	13347401	13347402	A	C	36	GENIC	homozygous	115260521
12	13347895	13347896	G	C	25	GENIC	homozygous	115260523
12	13347912	13347913	T	A	22	GENIC	homozygous	115260525
12	13348821	13348822	A	T	27	GENIC	homozygous	115260531
12	13349125	13349126	G	T	22	GENIC	homozygous	115260533
12	13352412	13352413	T	C	28	GENIC	homozygous	115260535
12	13352478	13352479	C	G	32	GENIC	homozygous	115260537
12	13352496	13352497	A	G	23	GENIC	homozygous	115260539
12	13353851	13353852	A	G	35	GENIC	homozygous	115260541
12	13355794	13355795	G	A	13	GENIC	possibly homozygous	115260545
12	13356239	13356240	T	C	23	GENIC	homozygous	115260547
12	13356270	13356271	A	G	25	GENIC	homozygous	115260549
12	13357430	13357431	A	T	25	GENIC	homozygous	115260551
12	13358926	13358927	C	T	33	GENIC	homozygous	115260553
12	13359335	13359336	C	A	30	GENIC	homozygous	115260555
12	13360505	13360506	T	C	36	GENIC	homozygous	115260557
12	13360656	13360657	G	A	21	GENIC	homozygous	115260559
12	13361674	13361675	C	T	14	GENIC	homozygous	115260561
12	13364325	13364326	A	C	22	GENIC	homozygous	115260563
12	13365385	13365386	G	T	31	GENIC	homozygous	115260565
12	13366011	13366012	G	A	30	GENIC	homozygous	115260567
12	13366979	13366980	C	T	23	GENIC	homozygous	115260569
12	13367214	13367215	G	A	25	GENIC	homozygous	115260571