chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40476111	40476112	T	-	26	GENIC	homozygous	50203611
12	40476210	40476211	C	A	26	GENIC	homozygous	50203612
12	40476211	40476212	T	C	26	GENIC	homozygous	50203613
12	40486483	40486484	T	-	23	GENIC	homozygous	50203621
12	40486487	40486488	T	C	24	GENIC	homozygous	50203622
12	40486490	40486491	G	T	26	GENIC	homozygous	50203623
12	40486514	40486515	T	C	27	GENIC	homozygous	50203624
12	40486525	40486526	A	T	32	GENIC	homozygous	50203625
12	40486549	40486550	G	A	31	GENIC	homozygous	50203626
12	40486553	40486554	G	T	32	GENIC	homozygous	50203627
12	40486582	40486583	T	TG	41	GENIC	homozygous	50203628
12	40486587	40486588	A	-	41	GENIC	homozygous	50203629
12	40486902	40486904	AC	--	7	GENIC	heterozygous	50610458