chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	27131009	27131010	T	C	15	GENIC	homozygous	50152504
12	27131019	27131020	G	A	16	GENIC	homozygous	50485206
12	27131096	27131097	A	AAC	15	GENIC	homozygous	50152506
12	27131128	27131129	T	G	13	GENIC	homozygous	50152508
12	27131511	27131512	C	T	19	GENIC	homozygous	50405934
12	27131565	27131566	A	G	26	GENIC	homozygous	50152510
12	27132168	27132169	G	T	14	GENIC	homozygous	50152512
12	27132264	27132265	C	T	14	GENIC	homozygous	50405938
12	27132737	27132738	T	C	11	GENIC	homozygous	50405939
12	27133430	27133431	A	T	13	GENIC	homozygous	50152516
12	27133590	27133591	T	C	17	GENIC	homozygous	50152518
12	27134161	27134162	T	C	11	GENIC	homozygous	50152520
12	27134976	27134977	A	G	7	GENIC	homozygous	50152537
12	27134991	27134992	T	C	7	GENIC	homozygous	50152539
12	27135167	27135168	A	G	11	GENIC	homozygous	50152547
12	27135406	27135408	AT	--	14	GENIC	homozygous	50152549
12	27136658	27136659	G	A	11	GENIC	homozygous	50152551
12	27136705	27136706	T	C	11	GENIC	homozygous	50152553
12	27137687	27137688	G	C	11	GENIC	homozygous	50485212
12	27140159	27140160	G	A	11	GENIC	homozygous	50419887
12	27141575	27141576	G	A	11	GENIC	homozygous	50485216
12	27142861	27142862	G	A	20	GENIC	homozygous	50485218
12	27142948	27142949	T	-	9	GENIC	homozygous	50152593
12	27143290	27143291	A	G	14	GENIC	homozygous	50152595