chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40347980	40347981	T	-	5	GENIC	heterozygous	50203300
12	40349985	40349987	CA	--	8	GENIC	heterozygous	50655145
12	40351369	40351370	C	CTT	7	GENIC	heterozygous	50855090
12	40358199	40358200	T	TC	14	GENIC	homozygous	50203380
12	40358206	40358207	T	TC	14	GENIC	homozygous	50203381
12	40358210	40358211	G	GC	14	GENIC	homozygous	50203382
12	40358269	40358270	C	CTG	7	GENIC	heterozygous	50563489
12	40358280	40358282	TG	--	7	GENIC	heterozygous	50543605
12	40358443	40358444	C	G	11	GENIC	homozygous	50203387
12	40358445	40358446	C	G	10	GENIC	homozygous	50203388
12	40363888	40363889	A	AGT	2	GENIC	heterozygous	50763022
12	40363105	40363106	T	-	23	GENIC	heterozygous	50512423