chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	43384883	43384884	G	A	45	GENIC	homozygous	139526647
14	43385350	43385351	G	A	30	GENIC	possibly homozygous	139526648
14	43385824	43385825	C		47	GENIC	homozygous	139395956
14	43386740	43386741	A	G	48	GENIC	homozygous	139526649
14	43387221	43387222	A	C	52	GENIC	homozygous	139526650
14	43387222	43387223	G	A	52	GENIC	homozygous	139526651
14	43387319	43387320	C	T	42	GENIC	homozygous	139526652
14	43388668	43388669	T	C	51	GENIC	homozygous	139526653
14	43388728	43388728		T	34	GENIC	possibly homozygous	139395957
14	43389231	43389231		C	44	GENIC	homozygous	139395958
14	43389496	43389500	CCCT		11	GENIC	homozygous	139395959
14	43389565	43389566	A	G	26	GENIC	possibly homozygous	139526654
14	43390378	43390379	G	A	46	GENIC	homozygous	139526655
14	43392338	43392338		C	21	GENIC	heterozygous	139395960
14	43393241	43393242	G	T	48	GENIC	homozygous	139526656
14	43393825	43393826	C	T	47	GENIC	homozygous	139526657
14	43394604	43394605	G	A	67	GENIC	possibly homozygous	147875243