chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	39660573	39660574	G	GT	4	GENIC	homozygous	51423901
10	39660585	39660586	G	T	7	GENIC	heterozygous	51423903
10	39661800	39661801	C	A	1	GENIC	homozygous	51858028
10	39664315	39664316	T	C	31	GENIC	possibly homozygous	51423906
10	39664670	39664673	CCC	---	6	GENIC	heterozygous	51423907
10	39666357	39666358	T	-	4	GENIC	heterozygous	51423908
10	39670058	39670059	A	-	4	GENIC	heterozygous	51423910
10	39671271	39671272	A	AT	6	GENIC	heterozygous	52044416
10	39671439	39671440	G	A	13	GENIC	possibly homozygous	51423911
10	39673198	39673199	G	A	7	GENIC	heterozygous	51423915
10	39676546	39676547	C	T	19	GENIC	possibly homozygous	51423922
10	39678202	39678204	AA	--	3	GENIC	heterozygous	51423923
10	39678203	39678204	A	-	3	GENIC	heterozygous	51423924
10	39687129	39687130	T	-	5	GENIC	heterozygous	52044446
10	39688462	39688463	T	C	16	GENIC	heterozygous	51423927
10	39688849	39688850	A	-	2	GENIC	homozygous	51423928
10	39691420	39691421	C	T	6	GENIC	heterozygous	51423929
10	39691450	39691451	C	T	13	GENIC	homozygous	51423930
10	39693211	39693212	C	-	12	GENIC	heterozygous	51423932
10	39693271	39693272	C	CGTGTGTGTGTGTGT	2	GENIC	heterozygous	52494351
10	39693306	39693307	C	-	4	GENIC	heterozygous	51423933
10	39693308	39693309	T	-	4	GENIC	heterozygous	51423934
10	39693314	39693315	A	-	3	GENIC	heterozygous	51423935
10	39693367	39693368	T	-	10	GENIC	homozygous	51423936
10	39693386	39693387	C	-	5	GENIC	homozygous	51423937
10	39697074	39697075	T	C	11	GENIC	homozygous	51423939
10	39703624	39703625	C	T	19	GENIC	homozygous	51423940
10	39705173	39705174	T	A	14	GENIC	homozygous	51423941
10	39708842	39708843	C	-	4	GENIC	heterozygous	51423943
10	39708842	39708843	C	A	4	GENIC	heterozygous	52437463
10	39715693	39715694	C	CA	2	GENIC	heterozygous	52044492
10	39715694	39715695	A	-	2	GENIC	heterozygous	51423949