chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	7631684	7631685	G	T	16	GENIC	homozygous	113326005
14	7657050	7657051	T	G	23	GENIC	homozygous	113326006
14	7657133	7657134	C	T	10	GENIC	homozygous	113326007
14	7657938	7657939	T	G	18	GENIC	homozygous	113326008
14	7658309	7658310	A	G	22	GENIC	homozygous	113326009
14	7658487	7658488	A	G	26	GENIC	homozygous	113326010
14	7658676	7658677	T	C	22	GENIC	homozygous	113326011
14	7658837	7658838	C	T	17	GENIC	homozygous	113326012
14	7659447	7659448	T	C	19	GENIC	homozygous	113326013
14	7659454	7659455	T	C	19	GENIC	homozygous	113326014
14	7659573	7659574	G	A	24	GENIC	homozygous	113326015
14	7659788	7659789	G	T	29	GENIC	homozygous	113326016
14	7677049	7677050	T	C	19	GENIC	homozygous	113326020
14	7658601	7658602	T	C	14	GENIC	homozygous	113572888
14	7673132	7673133	G	A	15	GENIC	homozygous	113572889
14	7679284	7679285	C	A	17	GENIC	homozygous	113572894
14	7679295	7679296	T	C	16	GENIC	homozygous	113326022
14	7679476	7679477	C	T	22	GENIC	homozygous	113326024
14	7681850	7681851	A	G	23	GENIC	homozygous	113326027
14	7682341	7682342	T	C	9	GENIC	homozygous	113326028