chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	160180921	160180922	G	C	9	GENIC	homozygous	59188535
2	160180923	160180924	G	C	9	GENIC	homozygous	59188536
2	160181650	160181651	T	A	21	GENIC	possibly homozygous	60678805
2	160182271	160182272	T	C	17	GENIC	possibly homozygous	59188543
2	160183260	160183261	T	G	2	GENIC	homozygous	60678807
2	160183632	160183633	G	A	16	GENIC	heterozygous	60678809
2	160183762	160183766	AAAC	----	7	GENIC	homozygous	60678811
2	160184539	160184540	G	C	22	GENIC	homozygous	60678813
2	160184752	160184753	C	T	3	GENIC	homozygous	60678815
2	160185196	160185197	T	C	9	GENIC	homozygous	60678817
2	160186201	160186202	A	G	14	GENIC	homozygous	60678819
2	160186732	160186733	C	T	18	GENIC	homozygous	60678821
2	160187316	160187317	A	G	25	GENIC	possibly homozygous	60678823
2	160187944	160187949	TCCCC	-----	9	GENIC	homozygous	60678825
2	160187951	160187952	C	A	7	GENIC	homozygous	60678827
2	160188405	160188406	T	C	21	GENIC	possibly homozygous	60678829
2	160188828	160188829	A	C	18	GENIC	homozygous	60678831
2	160189218	160189219	G	A	22	GENIC	possibly homozygous	60678833
2	160190946	160190947	G	GA	2	GENIC	heterozygous	60678835
2	160191138	160191139	T	TC	14	GENIC	possibly homozygous	60678837
2	160191394	160191395	T	C	25	GENIC	homozygous	60678839
2	160191536	160191537	G	A	3	GENIC	heterozygous	60678842
2	160192046	160192047	T	C	15	GENIC	homozygous	60678844
2	160192257	160192258	C	T	15	GENIC	possibly homozygous	60678846
2	160192309	160192310	T	TC	2	GENIC	homozygous	60678848
2	160192557	160192558	T	C	19	GENIC	possibly homozygous	59188550
2	160193855	160193862	CACGGGT	-------	2	GENIC	heterozygous	60678850
2	160197090	160197091	G	A	1	GENIC	homozygous	59188563
2	160197757	160197758	A	ATAGG	7	GENIC	homozygous	60678852
2	160198687	160198688	G	-	15	GENIC	homozygous	59188570
2	160200211	160200212	T	C	24	GENIC	possibly homozygous	59188574
2	160202490	160202491	T	C	22	GENIC	homozygous	59188577