chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40418430	40418431	G	GT	22	INTERGENIC	homozygous	50203518
12	40418549	40418550	T	C	20	INTERGENIC	homozygous	50203521
12	40418570	40418571	G	T	23	INTERGENIC	homozygous	50203522
12	40418583	40418584	C	A	23	INTERGENIC	homozygous	50512429
12	40418584	40418585	T	C	23	INTERGENIC	homozygous	50512431
12	40418592	40418593	G	GT	26	INTERGENIC	homozygous	50203523
12	40418609	40418610	C	-	30	INTERGENIC	homozygous	50203524
12	40418613	40418614	C	A	32	INTERGENIC	homozygous	50381644
12	40418656	40418657	G	-	38	INTERGENIC	homozygous	50203525
12	40418947	40418949	AA	--	16	INTERGENIC	heterozygous	50422631
12	40418948	40418949	A	-	16	INTERGENIC	possibly homozygous	50203527
12	40419336	40419337	C	CAGAATA	1	INTERGENIC	homozygous	50203528
12	40424766	40424767	T	TTG	9	INTERGENIC	homozygous	50600909
12	40428319	40428321	AA	--	9	INTERGENIC	heterozygous	50203536
12	40428320	40428321	A	-	9	INTERGENIC	possibly homozygous	50203537
12	40431118	40431119	C	-	3	INTERGENIC	heterozygous	50512433
12	40431434	40431436	TG	--	2	INTERGENIC	homozygous	50203545
12	40432468	40432469	T	-	15	INTERGENIC	heterozygous	50323280
12	40433323	40433324	A	G	22	INTERGENIC	homozygous	50452210
12	40455673	40455674	A	AACACACAC	13	GENIC	heterozygous	50543626
12	40455673	40455674	A	AAC	13	GENIC	heterozygous	50599318
12	40458615	40458616	T	C	16	GENIC	homozygous	50203574
12	40460022	40460023	T	TAC	16	GENIC	heterozygous	50694290
12	40460031	40460033	AC	--	16	GENIC	heterozygous	50694293
12	40444507	40444508	C	T	29	GENIC	homozygous	50948318
12	40445410	40445411	C	T	16	GENIC	homozygous	50948321
12	40455707	40455708	C	CAAAT	10	GENIC	homozygous	50948324