chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	41485285	41485286	G	A	12	GENIC	homozygous	139523741
14	41485297	41485298	G	A	11	GENIC	homozygous	139523742
14	41485540	41485541	A		16	GENIC	heterozygous	142420827
14	41485540	41485541	A	G	16	GENIC	homozygous	154855808
14	41485597	41485598	A	G	13	GENIC	homozygous	139523743
14	41487009	41487010	A	G	15	GENIC	homozygous	139523749
14	41487401	41487402	A	G	11	GENIC	homozygous	139523752
14	41488702	41488703	T	C	20	GENIC	homozygous	139523756
14	41490074	41490075	T	A	22	GENIC	homozygous	139523761
14	41490084	41490084		CTA	23	GENIC	homozygous	139395192
14	41486756	41486770	TTAACATATACCCA		14	GENIC	homozygous	144941982
14	41487139	41487140	G		19	GENIC	homozygous	144941983
14	41488649	41488649		GG	17	GENIC	homozygous	139395191
14	41490808	41490809	G		24	GENIC	homozygous	144941984
14	41490895	41490895		C	20	GENIC	homozygous	139395193
14	41491437	41491437		TGGGGGC	2	GENIC	homozygous	147833082
14	41491441	41491441		G	2	GENIC	homozygous	147833083
14	41491918	41491919	C		13	GENIC	homozygous	139395194
14	41492231	41492232	G	A	12	GENIC	homozygous	139523765
14	41493465	41493466	A	C	13	GENIC	homozygous	139523767
14	41495007	41495007		AC	10	GENIC	possibly homozygous	144941985
14	41490214	41490215	G	A	24	GENIC	homozygous	144961687
14	41491755	41491756	C	T	15	GENIC	homozygous	144961688
14	41493799	41493800	C	T	10	GENIC	homozygous	144961689
14	41495053	41495054	C	G	15	GENIC	possibly homozygous	144961690
14	41492905	41492906	C		5	GENIC	homozygous	403358552
14	41492905	41492906	C	G	5	GENIC	heterozygous	403358553