chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	54187778	54187779	G	C	3	GENIC	homozygous	50260633
12	54188137	54188138	C	T	4	GENIC	homozygous	50260635
12	54188892	54188893	A	G	2	GENIC	homozygous	50547965
12	54188895	54188896	T	TTTAGCTCAG	2	GENIC	homozygous	50547966
12	54188900	54188901	T	TAGA	2	GENIC	homozygous	50547967
12	54188952	54188954	AA	--	7	GENIC	homozygous	50260641
12	54189116	54189117	C	CTTTT	4	GENIC	homozygous	50547969
12	54189473	54189474	C	A	14	GENIC	homozygous	50260645
12	54190301	54190302	A	-	13	GENIC	homozygous	50260647
12	54190412	54190413	C	G	6	GENIC	homozygous	50260648
12	54190692	54190693	G	GA	7	GENIC	homozygous	50260650
12	54191358	54191359	C	-	7	GENIC	heterozygous	50260654
12	54191901	54191903	TC	--	6	GENIC	heterozygous	50260656
12	54192545	54192546	T	TAA	2	GENIC	heterozygous	50260658
12	54192545	54192546	T	TAAA	2	GENIC	heterozygous	50260660
12	54192676	54192677	T	C	10	GENIC	homozygous	50260662
12	54193388	54193389	G	A	9	GENIC	homozygous	50260664
12	54193642	54193643	C	CT	7	GENIC	possibly homozygous	50260666
12	54193874	54193875	A	-	11	GENIC	homozygous	50260668
12	54194992	54195040	CTGCTTCAGGCTGCTGTGTACTAGCTGTCCTTGTGCCAGGCCCATCCC	------------------------------------------------	11	GENIC	homozygous	50514493
12	54195623	54195624	C	T	10	GENIC	homozygous	50260670
12	54195914	54195915	G	A	14	GENIC	homozygous	50260672
12	54196213	54196214	G	GAATA	6	GENIC	homozygous	50260674