chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40418430	40418431	G	GT	34	INTERGENIC	homozygous	50203518
12	40418549	40418550	T	C	25	INTERGENIC	homozygous	50203521
12	40418570	40418571	G	T	24	INTERGENIC	homozygous	50203522
12	40418583	40418584	C	A	22	INTERGENIC	homozygous	50512429
12	40418584	40418585	T	C	22	INTERGENIC	homozygous	50512431
12	40418592	40418593	G	GT	25	INTERGENIC	homozygous	50203523
12	40418609	40418610	C	-	24	INTERGENIC	homozygous	50203524
12	40418613	40418614	C	A	25	INTERGENIC	homozygous	50381644
12	40418656	40418657	G	-	32	INTERGENIC	homozygous	50203525
12	40419336	40419337	C	CAGAATA	10	INTERGENIC	homozygous	50203528
12	40419385	40419386	A	T	8	INTERGENIC	homozygous	50203529
12	40424766	40424767	T	TTG	8	INTERGENIC	heterozygous	50600909
12	40424767	40424769	TG	--	8	INTERGENIC	heterozygous	50694231
12	40431118	40431119	C	-	10	INTERGENIC	heterozygous	50512433
12	40433323	40433324	A	G	33	INTERGENIC	homozygous	50452210
12	40456384	40456385	C	CA	22	GENIC	heterozygous	50203572
12	40460022	40460023	T	TAC	9	GENIC	heterozygous	50694290
12	40460031	40460033	AC	--	9	GENIC	heterozygous	50694293
12	40432468	40432469	T	-	23	INTERGENIC	heterozygous	50323280