chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	53531755	53531756	A	G	10	GENIC	homozygous	51648398
10	53532347	53532348	A	-	7	GENIC	heterozygous	52158407
10	53534241	53534242	A	G	20	GENIC	possibly homozygous	51648400
10	53535028	53535029	T	-	14	GENIC	homozygous	51648401
10	53535486	53535487	G	A	10	GENIC	homozygous	51648403
10	53535659	53535660	T	C	16	GENIC	homozygous	51648404
10	53537873	53537874	G	GTC	1	GENIC	homozygous	52460357
10	53547577	53547578	T	C	2	GENIC	homozygous	51648418
10	53550688	53550689	T	C	4	GENIC	homozygous	52057578
10	53550835	53550836	G	A	15	GENIC	possibly homozygous	52057580
10	53550964	53550983	CATGCGGTTACTCATCCAA	-------------------	3	GENIC	homozygous	52057582
10	53551009	53551010	G	A	10	GENIC	homozygous	52057584
10	53551066	53551067	T	A	15	GENIC	homozygous	52057586
10	53551123	53551124	G	GTCA	7	GENIC	homozygous	52057588
10	53551145	53551146	T	C	4	GENIC	homozygous	52057590
10	53551160	53551161	G	A	6	GENIC	homozygous	52057592
10	53551255	53551256	G	A	4	GENIC	homozygous	51648421
10	53551295	53551296	A	-	1	GENIC	homozygous	52057598
10	53551699	53551700	T	A	3	GENIC	homozygous	52057610
10	53551701	53551702	A	G	3	GENIC	homozygous	52318756
10	53551856	53551857	G	C	7	GENIC	homozygous	52057612
10	53551859	53551860	G	A	7	GENIC	homozygous	52057614
10	53551862	53551863	T	G	8	GENIC	homozygous	52057616
10	53552079	53552081	TT	--	4	GENIC	homozygous	52057618
10	53552473	53552474	A	G	9	GENIC	possibly homozygous	52057624
10	53552508	53552509	A	ATG	11	GENIC	heterozygous	52057626
10	53552972	53552973	A	G	20	GENIC	homozygous	52057628
10	53553071	53553072	G	T	11	GENIC	homozygous	52057630
10	53553072	53553073	A	T	11	GENIC	homozygous	52057632
10	53553117	53553118	T	-	15	GENIC	homozygous	52057634
10	53553729	53553730	A	C	3	GENIC	homozygous	51455620