chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	259779217	259779218	C	T	6	GENIC	homozygous	111198997
2	259779647	259779648	G	C	29	GENIC	homozygous	110421779
2	259779831	259779832	C	T	49	GENIC	homozygous	110421781
2	259780089	259780090	G	C	34	GENIC	homozygous	111198999
2	259780259	259780260	T	A	34	GENIC	homozygous	111199001
2	259780486	259780487	C	G	33	GENIC	homozygous	111199003
2	259780642	259780643	C	T	51	GENIC	homozygous	111046859
2	259780795	259780796	A	G	35	GENIC	homozygous	110421784
2	259780820	259780821	G	A	39	GENIC	homozygous	111199005
2	259782138	259782139	G	C	34	GENIC	homozygous	110421794
2	259782140	259782141	T	G	35	GENIC	homozygous	110421796
2	259782398	259782399	T	A	28	GENIC	homozygous	110421798
2	259782884	259782885	G	A	48	GENIC	homozygous	110421800
2	259783002	259783003	G	C	40	GENIC	homozygous	110421802
2	259783103	259783104	A	G	28	GENIC	homozygous	110421804
2	259783355	259783356	A	C	43	GENIC	homozygous	111199013
2	259783381	259783382	G	A	39	GENIC	homozygous	110421806
2	259783516	259783517	G	T	35	GENIC	homozygous	110421808
2	259783661	259783662	C	T	37	GENIC	homozygous	110421810
2	259784253	259784254	C	T	19	GENIC	homozygous	111199015
2	259784689	259784690	C	T	34	GENIC	homozygous	110421814