chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40476111	40476112	T	-	16	GENIC	homozygous	50203611
12	40486483	40486484	T	-	15	GENIC	homozygous	50203621
12	40486487	40486488	T	C	16	GENIC	possibly homozygous	50203622
12	40486490	40486491	G	T	16	GENIC	possibly homozygous	50203623
12	40486514	40486515	T	C	16	GENIC	homozygous	50203624
12	40486525	40486526	A	T	19	GENIC	possibly homozygous	50203625
12	40486549	40486550	G	A	21	GENIC	homozygous	50203626
12	40486553	40486554	G	T	23	GENIC	homozygous	50203627
12	40486582	40486583	T	TG	28	GENIC	homozygous	50203628
12	40486587	40486588	A	-	26	GENIC	homozygous	50203629