chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	80253163	80253164	G	C	22	GENIC	possibly homozygous	113500546
14	80253821	80253822	C	T	30	GENIC	possibly homozygous	113500547
14	80253891	80253892	G	A	27	GENIC	possibly homozygous	113500548
14	80254039	80254040	T	C	30	GENIC	homozygous	113500549
14	80254349	80254350	A	G	19	GENIC	possibly homozygous	113500550
14	80257085	80257086	T	C	25	GENIC	homozygous	113500551
14	80257560	80257561	A	G	26	GENIC	possibly homozygous	113500552
14	80260166	80260167	T	C	20	GENIC	homozygous	113500553
14	80260623	80260624	A	G	26	GENIC	homozygous	113500554
14	80261656	80261657	G	A	22	GENIC	possibly homozygous	113500555
14	80262193	80262194	G	A	22	GENIC	homozygous	113500556
14	80262475	80262476	A	G	19	GENIC	possibly homozygous	113500557
14	80263539	80263540	G	A	22	GENIC	possibly homozygous	113824151
14	80264836	80264837	C	T	22	GENIC	possibly homozygous	113500558
14	80268673	80268674	G	A	24	GENIC	possibly homozygous	113500559
14	80269627	80269628	G	A	27	GENIC	possibly homozygous	113500560
14	80269674	80269675	C	G	30	GENIC	homozygous	113876309
14	80270011	80270012	C	T	32	GENIC	homozygous	113500561
14	80270511	80270512	T	C	26	GENIC	possibly homozygous	113500562
14	80271100	80271101	T	G	27	GENIC	homozygous	113500563
14	80271102	80271103	G	T	26	GENIC	homozygous	113500564
14	80271863	80271864	T	G	26	GENIC	homozygous	113500565
14	80272095	80272096	A	G	41	GENIC	possibly homozygous	113500566
14	80274167	80274168	C	T	17	GENIC	homozygous	113500567
14	80274246	80274247	A	G	25	GENIC	possibly homozygous	113500568
14	80274359	80274360	A	G	9	GENIC	homozygous	113500569
14	80274542	80274543	A	G	20	GENIC	homozygous	113500570
14	80274778	80274779	C	T	19	GENIC	possibly homozygous	113500571
14	80274792	80274793	G	A	16	GENIC	possibly homozygous	113500572