chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	41059149	41059150	C	CTGCAGA	21	GENIC	homozygous	50205308
12	41059251	41059252	A	AAT	19	GENIC	homozygous	50205310
12	41059696	41059697	C	A	18	GENIC	homozygous	50205314
12	41060156	41060157	A	G	15	GENIC	homozygous	50205315
12	41060288	41060289	C	G	12	GENIC	homozygous	50323711
12	41060301	41060302	G	GTTTTT	4	GENIC	heterozygous	50610494
12	41060765	41060766	G	A	28	GENIC	homozygous	50205317
12	41061301	41061302	G	A	25	GENIC	homozygous	50205319
12	41061848	41061855	TTTTTGT	-------	19	GENIC	possibly homozygous	50205320
12	41062270	41062271	G	-	16	GENIC	homozygous	50205322
12	41062322	41062323	T	C	23	GENIC	possibly homozygous	50205323
12	41062372	41062373	T	C	22	GENIC	homozygous	50323713
12	41062401	41062402	A	G	22	GENIC	homozygous	50323715
12	41064833	41064834	A	G	12	GENIC	homozygous	50205328
12	41064973	41064985	ATTTATTTATTT	------------	11	GENIC	homozygous	50323717
12	41065303	41065304	T	A	17	GENIC	homozygous	50323719
12	41067226	41067227	A	-	13	GENIC	homozygous	50205333
12	41067427	41067428	A	AATAT	9	GENIC	homozygous	50205335
12	41067448	41067450	GG	--	5	GENIC	heterozygous	50205336
12	41067463	41067464	C	T	4	GENIC	homozygous	50323726
12	41067489	41067490	C	G	5	GENIC	homozygous	50205341
12	41067494	41067495	C	T	5	GENIC	homozygous	50205342
12	41067697	41067701	AAAG	----	22	GENIC	homozygous	50323728
12	41067812	41067813	T	C	21	GENIC	homozygous	50205343
12	41068014	41068015	C	CA	15	GENIC	homozygous	50323730
12	41076320	41076321	C	G	12	GENIC	homozygous	50205345
12	41060301	41060302	G	GTTTT	4	GENIC	heterozygous	50599343
12	41076273	41076297	ACACACACACACACACACACACAC	------------------------	16	GENIC	homozygous	50543826