chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	41059149	41059150	C	CTGCAGA	23	GENIC	homozygous	50205308
12	41059494	41059495	G	A	27	GENIC	homozygous	50381769
12	41059532	41059533	A	C	35	GENIC	homozygous	50381770
12	41059696	41059697	C	A	22	GENIC	homozygous	50205314
12	41060156	41060157	A	G	13	GENIC	homozygous	50205315
12	41060307	41060308	T	TG	11	GENIC	possibly homozygous	50381771
12	41060765	41060766	G	A	19	GENIC	homozygous	50205317
12	41062270	41062271	G	-	14	GENIC	homozygous	50205322
12	41062277	41062278	C	T	13	GENIC	homozygous	50381772
12	41062322	41062323	T	C	15	GENIC	homozygous	50205323
12	41062372	41062373	T	C	11	GENIC	homozygous	50323713
12	41063130	41063131	T	C	27	GENIC	homozygous	50381773
12	41064833	41064834	A	G	20	GENIC	homozygous	50205328
12	41065199	41065200	G	A	32	GENIC	homozygous	50381774
12	41066688	41066689	C	T	17	GENIC	homozygous	50381775
12	41066704	41066705	A	-	13	GENIC	possibly homozygous	50205332
12	41067448	41067450	GG	--	3	GENIC	homozygous	50205336
12	41067463	41067464	C	T	3	GENIC	homozygous	50323726
12	41067489	41067490	C	G	1	GENIC	homozygous	50205341
12	41067494	41067495	C	T	1	GENIC	homozygous	50205342
12	41076949	41076950	A	ACACACACACACACACACACACACTCT	12	GENIC	homozygous	50592143