chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	46072920	46072921	G	GT	19	GENIC	heterozygous	51444001
10	46073798	46073799	C	CTTTTTT	8	GENIC	homozygous	52373364
10	46075963	46075964	C	-	20	GENIC	homozygous	51444005
10	46075968	46075969	C	-	21	GENIC	homozygous	51444006
10	46075976	46075977	C	-	22	GENIC	homozygous	51444007
10	46075983	46075984	C	-	22	GENIC	homozygous	51444008
10	46076001	46076002	T	-	21	GENIC	homozygous	51444009
10	46076011	46076012	G	-	21	GENIC	homozygous	51444010
10	46076017	46076018	C	-	21	GENIC	homozygous	51444011
10	46076023	46076024	C	-	17	GENIC	homozygous	51444012
10	46076030	46076031	G	-	19	GENIC	homozygous	51444013
10	46076036	46076039	GAC	---	21	GENIC	homozygous	51444014
10	46076083	46076086	TTT	---	8	GENIC	heterozygous	52439055
10	46076306	46076307	G	A	26	GENIC	homozygous	51636651
10	46076423	46076424	A	G	15	GENIC	homozygous	51636652
10	46077068	46077069	G	A	14	GENIC	homozygous	51636653
10	46077072	46077073	C	CTTTTT	12	GENIC	homozygous	52647991
10	46077762	46077763	C	T	24	GENIC	homozygous	51636654
10	46078913	46078914	T	A	29	GENIC	homozygous	51636655
10	46079454	46079455	T	-	22	GENIC	homozygous	51444016
10	46081792	46081793	C	T	27	GENIC	homozygous	51636656
10	46083237	46083238	A	AT	25	GENIC	homozygous	51636657
10	46083338	46083339	C	T	31	GENIC	homozygous	51636658
10	46084205	46084206	A	G	23	GENIC	homozygous	51636659
10	46084323	46084324	T	G	17	GENIC	homozygous	51444019
10	46085224	46085225	C	T	12	GENIC	homozygous	51636660
10	46085981	46085982	G	A	25	GENIC	homozygous	51636661