chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	7631684	7631685	G	T	23	GENIC	homozygous	113326005
14	7657133	7657134	C	T	12	GENIC	homozygous	113326007
14	7658487	7658488	A	G	14	GENIC	homozygous	113326010
14	7658676	7658677	T	C	27	GENIC	homozygous	113326011
14	7659447	7659448	T	C	12	GENIC	homozygous	113326013
14	7659454	7659455	T	C	12	GENIC	homozygous	113326014
14	7659788	7659789	G	T	12	GENIC	homozygous	113326016
14	7658738	7658739	T	C	22	GENIC	homozygous	113643985
14	7658601	7658602	T	C	20	GENIC	homozygous	113572888
14	7660466	7660467	G	A	26	GENIC	homozygous	114095984
14	7677049	7677050	T	C	20	GENIC	homozygous	113326020
14	7678281	7678282	C	A	29	GENIC	homozygous	113802855
14	7678624	7678625	T	C	28	GENIC	homozygous	113802857
14	7679295	7679296	T	C	25	GENIC	homozygous	113326022
14	7679476	7679477	C	T	19	GENIC	homozygous	113326024
14	7680587	7680588	G	A	21	GENIC	homozygous	113802861
14	7681700	7681701	C	T	23	GENIC	homozygous	113802863
14	7681850	7681851	A	G	23	GENIC	homozygous	113326027
14	7682341	7682342	T	C	7	GENIC	homozygous	113326028