chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	51801929	51801930	C	T	55	GENIC	possibly homozygous	112507977
15	51802395	51802396	A	C	52	GENIC	homozygous	112507979
15	51802953	51802954	G	A	59	GENIC	possibly homozygous	112507981
15	51803419	51803420	C	T	50	GENIC	homozygous	112507983
15	51805864	51805865	T	C	67	GENIC	homozygous	112507985
15	51806815	51806816	C	T	55	GENIC	possibly homozygous	112507987
15	51806841	51806842	C	T	52	GENIC	homozygous	112507989
15	51806929	51806930	G	A	43	GENIC	homozygous	113054368
15	51807617	51807618	C	T	36	GENIC	homozygous	112507991
15	51807840	51807841	G	T	43	GENIC	homozygous	112507993
15	51808850	51808851	A	G	43	GENIC	homozygous	112507995
15	51809057	51809058	C	T	36	GENIC	homozygous	112507997
15	51809112	51809113	A	G	49	GENIC	homozygous	112507999
15	51811100	51811101	C	T	45	GENIC	homozygous	112508001
15	51811192	51811193	T	G	34	GENIC	homozygous	112508003
15	51811999	51812000	C	T	33	GENIC	homozygous	112508005
15	51812762	51812763	C	T	51	GENIC	homozygous	112508007
15	51813857	51813858	T	C	60	GENIC	homozygous	112508009
15	51814251	51814252	T	C	64	GENIC	homozygous	112508011
15	51816549	51816550	T	C	62	GENIC	homozygous	112508013
15	51816708	51816709	G	A	41	GENIC	homozygous	112508015
15	51818487	51818488	C	T	51	GENIC	possibly homozygous	112508017
15	51818500	51818501	T	C	46	GENIC	homozygous	112508019