chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	41059149	41059150	C	CTGCAGA	10	GENIC	homozygous	50205308
12	41059150	41059151	G	T	11	GENIC	heterozygous	50205309
12	41059251	41059252	A	AAT	19	GENIC	possibly homozygous	50205310
12	41059252	41059253	A	AT	18	GENIC	heterozygous	50205311
12	41059253	41059254	G	GA	19	GENIC	possibly homozygous	50205313
12	41059696	41059697	C	A	20	GENIC	homozygous	50205314
12	41060156	41060157	A	G	16	GENIC	homozygous	50205315
12	41060288	41060289	C	G	23	GENIC	possibly homozygous	50323711
12	41060765	41060766	G	A	29	GENIC	homozygous	50205317
12	41061301	41061302	G	A	29	GENIC	homozygous	50205319
12	41061848	41061855	TTTTTGT	-------	18	GENIC	possibly homozygous	50205320
12	41061854	41061855	T	-	19	GENIC	possibly homozygous	50205321
12	41062270	41062271	G	-	16	GENIC	homozygous	50205322
12	41062322	41062323	T	C	26	GENIC	possibly homozygous	50205323
12	41062372	41062373	T	C	26	GENIC	homozygous	50323713
12	41062401	41062402	A	G	26	GENIC	homozygous	50323715
12	41064833	41064834	A	G	12	GENIC	homozygous	50205328
12	41064973	41064985	ATTTATTTATTT	------------	9	GENIC	homozygous	50323717
12	41065303	41065304	T	A	21	GENIC	homozygous	50323719
12	41067226	41067227	A	-	17	GENIC	homozygous	50205333
12	41067427	41067428	A	AATAT	7	GENIC	homozygous	50205335
12	41067442	41067443	G	A	8	GENIC	heterozygous	50323721
12	41067447	41067448	T	TG	3	GENIC	homozygous	50323723
12	41067468	41067469	C	-	1	GENIC	homozygous	50205338
12	41067478	41067479	G	A	7	GENIC	possibly homozygous	50205339
12	41067485	41067486	T	C	6	GENIC	homozygous	50205340
12	41067489	41067490	C	G	7	GENIC	homozygous	50205341
12	41067494	41067495	C	T	7	GENIC	homozygous	50205342
12	41067697	41067701	AAAG	----	20	GENIC	homozygous	50323728
12	41067812	41067813	T	C	18	GENIC	homozygous	50205343
12	41068014	41068015	C	CA	12	GENIC	homozygous	50323730
12	41076951	41076952	T	A	22	GENIC	heterozygous	50205348
12	41076953	41076954	T	A	20	GENIC	heterozygous	50205349