chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40695542	40695543	T	A	15	GENIC	possibly homozygous	50204344
12	40695955	40695956	C	G	14	GENIC	homozygous	50204345
12	40697877	40697878	T	C	19	GENIC	homozygous	50204348
12	40698161	40698162	A	G	15	GENIC	possibly homozygous	50204349
12	40698668	40698669	G	A	9	GENIC	homozygous	50204350
12	40698750	40698751	T	C	3	GENIC	homozygous	50204351
12	40699020	40699021	G	A	4	GENIC	homozygous	50204352
12	40699857	40699863	AGAAGG	------	1	INTERGENIC	homozygous	50204355
12	40701819	40701820	G	A	19	INTERGENIC	possibly homozygous	50204361
12	40701978	40701979	C	CA	4	INTERGENIC	homozygous	50204363
12	40701982	40701983	T	-	3	INTERGENIC	homozygous	50204364
12	40701984	40701985	T	C	2	INTERGENIC	homozygous	50204365
12	40702503	40702504	T	C	4	INTERGENIC	homozygous	50204372
12	40702923	40702924	C	T	25	INTERGENIC	possibly homozygous	50204373
12	40703583	40703584	C	CTT	2	INTERGENIC	heterozygous	50204374
12	40703583	40703584	C	CT	2	INTERGENIC	heterozygous	50640203
12	40704413	40704414	G	A	27	INTERGENIC	homozygous	50204375
12	40709100	40709101	T	C	8	INTERGENIC	homozygous	50204379