chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	1411480	1411481	C	T	14	GENIC	homozygous	120428332
2	1411569	1411570	T	G	18	GENIC	homozygous	120308889
2	1413704	1413705	A	G	27	GENIC	homozygous	120353768
2	1415149	1415150	T	C	17	GENIC	homozygous	120308891
2	1419344	1419345	T	G	25	GENIC	homozygous	120353769
2	1419355	1419356	A	G	26	GENIC	homozygous	120353770
2	1419402	1419403	T	C	25	GENIC	homozygous	120428333
2	1419418	1419419	A	G	25	GENIC	homozygous	120353771
2	1419435	1419436	T	C	29	GENIC	homozygous	120353772
2	1419818	1419819	C	T	23	GENIC	homozygous	120353773
2	1421517	1421518	C	A	16	GENIC	homozygous	120428334
2	1423693	1423694	G	A	24	GENIC	homozygous	120308893
2	1424037	1424038	C	T	23	GENIC	homozygous	120353774
2	1427296	1427297	T	C	24	GENIC	homozygous	120308894
2	1429695	1429696	G	A	23	GENIC	homozygous	120308895
2	1430013	1430014	G	A	13	GENIC	homozygous	120308896
2	1445889	1445890	C	G	25	GENIC	homozygous	120308897
2	1447182	1447183	T	C	24	GENIC	homozygous	120308898
2	1447804	1447805	C	A	14	GENIC	homozygous	120308899
2	1447807	1447808	C	A	20	GENIC	homozygous	120308900
2	1448290	1448291	C	T	27	GENIC	homozygous	120308901