chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	13672605	13672606	G	A	24	GENIC	homozygous	51621900
10	13673047	13673048	T	C	24	GENIC	homozygous	51621901
10	13673295	13673296	C	-	21	GENIC	homozygous	51621902
10	13673310	13673311	A	C	16	GENIC	homozygous	51621903
10	13674419	13674420	G	GAAAAAAAAAAAA	7	GENIC	homozygous	52313013
10	13674422	13674423	G	GAAGA	7	GENIC	homozygous	52313014
10	13675013	13675014	C	T	40	GENIC	homozygous	51621905
10	13675929	13675931	AA	--	11	GENIC	heterozygous	52431432
10	13675930	13675931	A	-	11	GENIC	heterozygous	52431434
10	13676018	13676019	T	TGA	5	GENIC	heterozygous	52481187
10	13676081	13676082	A	G	27	GENIC	homozygous	51621909
10	13676212	13676213	C	T	26	GENIC	homozygous	51621910
10	13676420	13676421	T	TTC	9	GENIC	heterozygous	51621911
10	13676426	13676427	C	-	8	GENIC	heterozygous	52356463
10	13676430	13676433	TTC	---	8	GENIC	heterozygous	52431436
10	13676857	13676858	C	T	34	GENIC	homozygous	51621912
10	13677051	13677052	T	C	18	GENIC	homozygous	51621913
10	13677072	13677073	C	CGTGTGTGTGTGTGTGT	6	GENIC	homozygous	52431438
10	13677288	13677289	A	C	24	GENIC	homozygous	51621914
10	13677743	13677744	C	-	8	GENIC	homozygous	51621915
10	13680278	13680279	G	A	43	GENIC	homozygous	51621917
10	13680478	13680479	G	GCA	41	GENIC	possibly homozygous	51621918
10	13680660	13680662	AA	--	18	GENIC	homozygous	51621919
10	13680885	13680886	A	AAAAAAAAC	13	GENIC	homozygous	51621920
10	13680905	13680906	A	C	11	GENIC	homozygous	51621922
10	13681458	13681459	G	A	26	GENIC	homozygous	51621923
10	13682513	13682514	G	A	23	GENIC	possibly homozygous	51621924
10	13682848	13682849	G	A	38	GENIC	homozygous	51621925
10	13682928	13682929	C	T	31	GENIC	homozygous	51621926
10	13682935	13682936	T	G	30	GENIC	homozygous	51621927
10	13683164	13683165	G	A	28	GENIC	homozygous	51621928
10	13684315	13684316	G	A	30	GENIC	homozygous	51621929
10	13684808	13684809	A	G	18	GENIC	homozygous	51621930
10	13687593	13687594	C	T	22	GENIC	homozygous	51621931