chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	160018092	160018093	T	A	34	GENIC	homozygous	142953754
2	160018616	160018616		T	25	GENIC	homozygous	142898607
2	160019499	160019500	A		34	GENIC	homozygous	142898608
2	160021115	160021116	G	A	25	GENIC	possibly homozygous	142953755
2	160023647	160023648	A	C	47	GENIC	possibly homozygous	142953756
2	160024009	160024010	T	C	52	GENIC	homozygous	136342377
2	160024850	160024851	C	G	48	GENIC	homozygous	136342384
2	160026031	160026032	G	A	52	GENIC	homozygous	142953757
2	160026494	160026495	A	C	47	GENIC	homozygous	142953758
2	160027776	160027777	T	C	51	GENIC	homozygous	142953759
2	160027911	160027912	G	T	50	GENIC	homozygous	154003159
2	160027911	160027912	G	A	50	GENIC	heterozygous	154003160
2	160031628	160031629	A	G	51	GENIC	homozygous	136342397
2	160034115	160034116	T	C	44	GENIC	homozygous	142953760
2	160034534	160034535	A		57	GENIC	possibly homozygous	135954527
2	160035308	160035309	T	C	45	GENIC	homozygous	142953761
2	160035328	160035329	C	T	45	GENIC	homozygous	142953762
2	160036695	160036696	T	G	64	GENIC	homozygous	136342404
2	160037990	160037991	C	T	45	GENIC	homozygous	136342407
2	160039486	160039487	G		45	GENIC	homozygous	142898609
2	160041998	160041998		CT	47	GENIC	homozygous	135954531
2	160042480	160042480		CCCA	11	GENIC	homozygous	135954532
2	160043861	160043862	G	A	56	GENIC	homozygous	142953763
2	160044235	160044236	G	A	50	GENIC	homozygous	136342422