chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40469100	40469103	AAA	---	8	GENIC	heterozygous	50558979
12	40469102	40469103	A	-	8	GENIC	possibly homozygous	50563495
12	40476111	40476112	T	-	19	GENIC	homozygous	50203611
12	40476210	40476211	C	A	21	GENIC	homozygous	50203612
12	40476211	40476212	T	C	21	GENIC	homozygous	50203613
12	40476525	40476526	A	C	15	GENIC	homozygous	50203614
12	40482465	40482466	G	GGGCA	17	GENIC	homozygous	50948327
12	40482666	40482667	A	G	26	GENIC	homozygous	50948330
12	40486483	40486484	T	-	22	GENIC	homozygous	50203621
12	40486487	40486488	T	C	22	GENIC	homozygous	50203622
12	40486490	40486491	G	T	19	GENIC	homozygous	50203623
12	40486514	40486515	T	C	18	GENIC	homozygous	50203624
12	40486525	40486526	A	T	16	GENIC	homozygous	50203625
12	40486549	40486550	G	A	25	GENIC	homozygous	50203626
12	40486553	40486554	G	T	26	GENIC	homozygous	50203627
12	40486582	40486583	T	TG	16	GENIC	homozygous	50203628
12	40486587	40486588	A	-	16	GENIC	homozygous	50203629
12	40486893	40486894	T	TACAC	2	GENIC	homozygous	50571688
12	40489387	40489388	G	A	22	GENIC	homozygous	50948333
12	40490915	40490916	T	C	22	GENIC	homozygous	50203640
12	40492492	40492493	G	A	14	GENIC	homozygous	50203641