chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	7631684	7631685	G	T	33	GENIC	homozygous	113326005
14	7658487	7658488	A	G	25	GENIC	homozygous	113326010
14	7658676	7658677	T	C	37	GENIC	homozygous	113326011
14	7659447	7659448	T	C	17	GENIC	homozygous	113326013
14	7659454	7659455	T	C	16	GENIC	homozygous	113326014
14	7659788	7659789	G	T	30	GENIC	homozygous	113326016
14	7673208	7673209	T	C	26	GENIC	homozygous	113326017
14	7673229	7673230	C	A	35	GENIC	homozygous	113572891
14	7658738	7658739	T	C	22	GENIC	homozygous	113643985
14	7673224	7673225	T	G	32	GENIC	homozygous	113572890
14	7659854	7659855	C	T	14	GENIC	homozygous	113802853
14	7673274	7673275	T	C	36	GENIC	homozygous	113326018
14	7677049	7677050	T	C	41	GENIC	homozygous	113326020
14	7678281	7678282	C	A	31	GENIC	homozygous	113802855
14	7678624	7678625	T	C	30	GENIC	homozygous	113802857
14	7678925	7678926	T	C	21	GENIC	homozygous	113802859
14	7679295	7679296	T	C	25	GENIC	homozygous	113326022
14	7679476	7679477	C	T	36	GENIC	homozygous	113326024
14	7680587	7680588	G	A	20	GENIC	homozygous	113802861
14	7681700	7681701	C	T	26	GENIC	homozygous	113802863
14	7681850	7681851	A	G	27	GENIC	homozygous	113326027
14	7682341	7682342	T	C	29	GENIC	homozygous	113326028