chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	46071603	46071604	T	C	17	GENIC	homozygous	51444000
10	46072201	46072202	C	CT	6	GENIC	heterozygous	52439053
10	46072920	46072921	G	GT	11	GENIC	possibly homozygous	51444001
10	46073798	46073799	C	CTTTTTT	2	GENIC	heterozygous	52373364
10	46073799	46073803	TTTT	----	2	GENIC	heterozygous	51444003
10	46075963	46075964	C	-	18	GENIC	homozygous	51444005
10	46075968	46075969	C	-	19	GENIC	homozygous	51444006
10	46075976	46075977	C	-	17	GENIC	homozygous	51444007
10	46075983	46075984	C	-	17	GENIC	homozygous	51444008
10	46076001	46076002	T	-	18	GENIC	homozygous	51444009
10	46076011	46076012	G	-	19	GENIC	homozygous	51444010
10	46076017	46076018	C	-	17	GENIC	homozygous	51444011
10	46076023	46076024	C	-	17	GENIC	homozygous	51444012
10	46076030	46076031	G	-	15	GENIC	homozygous	51444013
10	46076036	46076039	GAC	---	15	GENIC	homozygous	51444014
10	46076208	46076209	G	T	11	GENIC	homozygous	51444015
10	46077072	46077073	C	CTTTTTTTT	3	GENIC	homozygous	52373366
10	46079454	46079455	T	-	21	GENIC	homozygous	51444016
10	46080883	46080884	T	C	27	GENIC	homozygous	51444017
10	46082696	46082697	C	T	20	GENIC	homozygous	51444018
10	46084323	46084324	T	G	31	GENIC	homozygous	51444019