chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	40467233	40467234	A	-	18	GENIC	homozygous	50422686
12	40467286	40467287	G	T	20	GENIC	homozygous	50422687
12	40467707	40467716	TCTGTTGTT	---------	17	GENIC	homozygous	50203601
12	40468063	40468064	G	A	7	GENIC	homozygous	50203604
12	40468308	40468309	T	C	14	GENIC	homozygous	50422689
12	40468446	40468447	G	C	18	GENIC	homozygous	50203605
12	40469452	40469453	T	A	10	GENIC	homozygous	50203607
12	40470888	40470889	C	T	19	GENIC	homozygous	50203610
12	40476111	40476112	T	-	20	GENIC	homozygous	50203611
12	40476210	40476211	C	A	16	GENIC	homozygous	50203612
12	40476211	40476212	T	C	16	GENIC	homozygous	50203613
12	40476525	40476526	A	C	24	GENIC	homozygous	50203614
12	40480166	40480167	C	T	23	GENIC	homozygous	51099742
12	40480365	40480366	G	A	14	GENIC	homozygous	51099744
12	40482279	40482280	G	A	9	GENIC	homozygous	51099746
12	40483102	40483103	C	A	21	GENIC	homozygous	50203617
12	40486483	40486484	T	-	19	GENIC	homozygous	50203621
12	40486487	40486488	T	C	18	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	11	GENIC	homozygous	50203626
12	40486553	40486554	G	T	11	GENIC	homozygous	50203627
12	40486582	40486583	T	TG	7	GENIC	homozygous	50203628
12	40486587	40486588	A	-	9	GENIC	homozygous	50203629
12	40490915	40490916	T	C	13	GENIC	homozygous	50203640
12	40492492	40492493	G	A	10	GENIC	homozygous	50203641
12	40495137	40495138	C	T	24	GENIC	homozygous	51099748