chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40695542	40695543	T	A	20	GENIC	homozygous	50204344
12	40695955	40695956	C	G	43	GENIC	homozygous	50204345
12	40696271	40696272	T	-	11	GENIC	heterozygous	50381663
12	40697264	40697265	G	GAA	28	GENIC	heterozygous	50204346
12	40697264	40697265	G	GA	28	GENIC	heterozygous	50204347
12	40697877	40697878	T	C	33	GENIC	homozygous	50204348
12	40698161	40698162	A	G	34	GENIC	homozygous	50204349
12	40698668	40698669	G	A	43	GENIC	homozygous	50204350
12	40698750	40698751	T	C	42	GENIC	homozygous	50204351
12	40699020	40699021	G	A	24	GENIC	homozygous	50204352
12	40699113	40699114	C	CT	13	GENIC	possibly homozygous	50204353
12	40699857	40699863	AGAAGG	------	16	INTERGENIC	homozygous	50204355
12	40699920	40699921	G	C	26	INTERGENIC	homozygous	50204356
12	40701819	40701820	G	A	38	INTERGENIC	homozygous	50204361
12	40701982	40701983	T	-	27	INTERGENIC	homozygous	50204364
12	40701978	40701979	C	CA	28	INTERGENIC	homozygous	50204363
12	40701984	40701985	T	C	25	INTERGENIC	homozygous	50204365
12	40702025	40702026	C	CA	11	INTERGENIC	heterozygous	50204366
12	40702453	40702454	T	TA	24	INTERGENIC	homozygous	50204370
12	40702468	40702469	G	-	28	INTERGENIC	homozygous	50204371
12	40702503	40702504	T	C	30	INTERGENIC	homozygous	50204372
12	40702923	40702924	C	T	42	INTERGENIC	homozygous	50204373
12	40703583	40703584	C	CTT	34	INTERGENIC	homozygous	50204374
12	40704413	40704414	G	A	31	INTERGENIC	homozygous	50204375
12	40709100	40709101	T	C	23	INTERGENIC	homozygous	50204379