chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40469101	40469103	AA	--	11	GENIC	heterozygous	50543630
12	40469102	40469103	A	-	11	GENIC	heterozygous	50563495
12	40476111	40476112	T	-	23	GENIC	homozygous	50203611
12	40476210	40476211	C	A	22	GENIC	homozygous	50203612
12	40476211	40476212	T	C	22	GENIC	homozygous	50203613
12	40476525	40476526	A	C	26	GENIC	homozygous	50203614
12	40482465	40482466	G	GGGCA	19	GENIC	homozygous	50948327
12	40482666	40482667	A	G	32	GENIC	homozygous	50948330
12	40486483	40486484	T	-	27	GENIC	homozygous	50203621
12	40486487	40486488	T	C	28	GENIC	homozygous	50203622
12	40486490	40486491	G	T	28	GENIC	homozygous	50203623
12	40486514	40486515	T	C	34	GENIC	homozygous	50203624
12	40486525	40486526	A	T	36	GENIC	homozygous	50203625
12	40486549	40486550	G	A	33	GENIC	homozygous	50203626
12	40486553	40486554	G	T	31	GENIC	homozygous	50203627
12	40486582	40486583	T	TG	34	GENIC	homozygous	50203628
12	40486587	40486588	A	-	36	GENIC	homozygous	50203629
12	40486893	40486894	T	TACAC	4	GENIC	homozygous	50571688
12	40489387	40489388	G	A	29	GENIC	homozygous	50948333
12	40490915	40490916	T	C	29	GENIC	homozygous	50203640
12	40492492	40492493	G	A	24	GENIC	homozygous	50203641