chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	27131009	27131010	T	C	18	GENIC	possibly homozygous	50152504
12	27131019	27131020	G	A	18	GENIC	homozygous	50485206
12	27131096	27131097	A	AAC	17	GENIC	homozygous	50152506
12	27131128	27131129	T	G	18	GENIC	possibly homozygous	50152508
12	27131511	27131512	C	T	18	GENIC	possibly homozygous	50405934
12	27131565	27131566	A	G	17	GENIC	possibly homozygous	50152510
12	27132168	27132169	G	T	22	GENIC	possibly homozygous	50152512
12	27132264	27132265	C	T	26	GENIC	homozygous	50405938
12	27132737	27132738	T	C	24	GENIC	homozygous	50405939
12	27133430	27133431	A	T	18	GENIC	possibly homozygous	50152516
12	27133590	27133591	T	C	16	GENIC	homozygous	50152518
12	27134161	27134162	T	C	38	GENIC	possibly homozygous	50152520
12	27134976	27134977	A	G	4	GENIC	homozygous	50152537
12	27135074	27135075	T	A	3	GENIC	heterozygous	50509540
12	27135086	27135087	A	-	2	GENIC	heterozygous	50405945
12	27135167	27135168	A	G	7	GENIC	homozygous	50152547
12	27135406	27135408	AT	--	11	GENIC	homozygous	50152549
12	27136658	27136659	G	A	30	GENIC	possibly homozygous	50152551
12	27136705	27136706	T	C	16	GENIC	homozygous	50152553
12	27137687	27137688	G	C	22	GENIC	possibly homozygous	50485212
12	27137921	27137922	C	CA	27	GENIC	homozygous	50152563
12	27138867	27138868	C	T	30	GENIC	possibly homozygous	50152569
12	27140159	27140160	G	A	10	GENIC	possibly homozygous	50419887
12	27140825	27140839	GTGTGTGTGTGTGT	--------------	1	GENIC	homozygous	50485214
12	27140875	27140876	T	C	34	GENIC	possibly homozygous	50152583
12	27141271	27141272	G	A	7	GENIC	homozygous	50440610
12	27141353	27141354	T	C	17	GENIC	homozygous	50152585
12	27141575	27141576	G	A	13	GENIC	possibly homozygous	50485216
12	27142861	27142862	G	A	17	GENIC	homozygous	50485218
12	27142948	27142949	T	-	3	GENIC	homozygous	50152593
12	27143290	27143291	A	G	8	GENIC	homozygous	50152595
12	27143517	27143518	C	CA	4	GENIC	heterozygous	50419890