chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	2066618	2066619	A	G	22	GENIC	possibly homozygous	48447578
14	2069006	2069007	C	A	11	GENIC	possibly homozygous	48447579
14	2069459	2069460	C	G	28	GENIC	homozygous	48447580
14	2069628	2069629	T	C	12	GENIC	possibly homozygous	48447581
14	2070293	2070294	G	A	28	GENIC	possibly homozygous	48447582
14	2070887	2070888	A	G	16	GENIC	possibly homozygous	48447583
14	2072586	2072587	A	G	25	GENIC	possibly homozygous	48447584
14	2072661	2072662	G	A	26	GENIC	homozygous	48447585
14	2072831	2072832	G	A	14	GENIC	homozygous	48447586
14	2072853	2072854	C	T	5	GENIC	homozygous	48447587
14	2073029	2073030	C	CT	21	GENIC	homozygous	48447588
14	2073812	2073813	G	A	24	GENIC	homozygous	48447590
14	2074136	2074137	A	G	24	GENIC	homozygous	48447591
14	2074210	2074211	C	T	20	GENIC	heterozygous	48447592
14	2074346	2074347	G	A	10	GENIC	heterozygous	48447593
14	2074411	2074412	C	T	16	GENIC	possibly homozygous	48447594
14	2074739	2074740	T	C	34	GENIC	possibly homozygous	48447595
14	2076011	2076012	T	C	23	GENIC	homozygous	48447596
14	2078633	2078634	A	G	23	GENIC	possibly homozygous	48447597
14	2078833	2078834	G	A	19	GENIC	homozygous	48447598
14	2078845	2078846	A	-	17	GENIC	homozygous	48447599