chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40341047	40341048	T	C	14	GENIC	homozygous	50203281
12	40341058	40341059	G	A	17	GENIC	homozygous	50203282
12	40341213	40341214	A	C	26	GENIC	homozygous	50422620
12	40341986	40341987	T	-	24	GENIC	homozygous	50203283
12	40342338	40342339	G	A	19	GENIC	homozygous	50203284
12	40342426	40342427	A	G	24	GENIC	homozygous	50203285
12	40342760	40342761	A	G	24	GENIC	homozygous	50203286
12	40347980	40347981	T	-	6	GENIC	heterozygous	50203300
12	40349984	40349985	G	GCACACACACACACACACA	9	GENIC	homozygous	50543603
12	40350849	40350851	CA	--	5	GENIC	heterozygous	50563487
12	40354386	40354387	G	A	21	GENIC	homozygous	50422621
12	40355056	40355060	GTGT	----	6	GENIC	homozygous	50543604
12	40358199	40358200	T	TC	27	GENIC	homozygous	50203380
12	40358206	40358207	T	TC	24	GENIC	homozygous	50203381
12	40358210	40358211	G	GC	21	GENIC	homozygous	50203382
12	40358269	40358270	C	CTG	9	GENIC	heterozygous	50563489
12	40358280	40358282	TG	--	9	GENIC	heterozygous	50543605
12	40358443	40358444	C	G	27	GENIC	homozygous	50203387
12	40358445	40358446	C	G	28	GENIC	homozygous	50203388
12	40359068	40359069	C	CA	31	GENIC	heterozygous	50599316
12	40363889	40363897	GTGTGTGT	--------	4	GENIC	heterozygous	50563491
12	40363893	40363897	GTGT	----	4	GENIC	heterozygous	50543606
12	40364121	40364122	A	-	10	GENIC	homozygous	50203393
12	40364774	40364775	C	T	31	GENIC	homozygous	50203396
12	40364782	40364783	A	C	32	GENIC	homozygous	50203397