chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	1411569	1411570	T	G	30	GENIC	homozygous	120308889
2	1413704	1413705	A	G	20	GENIC	homozygous	120353768
2	1415149	1415150	T	C	33	GENIC	homozygous	120308891
2	1419344	1419345	T	G	41	GENIC	homozygous	120353769
2	1419355	1419356	A	G	38	GENIC	homozygous	120353770
2	1419418	1419419	A	G	31	GENIC	homozygous	120353771
2	1419435	1419436	T	C	33	GENIC	homozygous	120353772
2	1419818	1419819	C	T	25	GENIC	homozygous	120353773
2	1423693	1423694	G	A	21	GENIC	homozygous	120308893
2	1424037	1424038	C	T	43	GENIC	homozygous	120353774
2	1427296	1427297	T	C	24	GENIC	homozygous	120308894
2	1429695	1429696	G	A	24	GENIC	homozygous	120308895
2	1430013	1430014	G	A	15	GENIC	homozygous	120308896
2	1439121	1439122	C	T	26	GENIC	homozygous	120353775
2	1447182	1447183	T	C	28	GENIC	homozygous	120308898
2	1448290	1448291	C	T	33	GENIC	homozygous	120308901
2	1449679	1449680	A	G	11	GENIC	homozygous	120353776
2	1443056	1443057	T	A	7	GENIC	homozygous	120386520