chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	44840970	44840971	T	C	60	GENIC	homozygous	136092101
2	44841305	44841306	T	C	47	GENIC	homozygous	136092102
2	44841547	44841548	C	T	49	GENIC	homozygous	136092103
2	44842414	44842415	C	T	48	GENIC	homozygous	143823197
2	44843004	44843005	T	C	45	GENIC	homozygous	136092104
2	44843275	44843275		CCATTGCGT	48	GENIC	homozygous	135903797
2	44843675	44843676	A		26	GENIC	homozygous	135903798
2	44843813	44843814	A	G	34	GENIC	homozygous	136092106
2	44844146	44844147	T	G	53	GENIC	homozygous	143823198
2	44844388	44844389	A	G	49	GENIC	homozygous	136092107
2	44844570	44844571	C	T	40	GENIC	homozygous	136092108
2	44844759	44844760	A	G	23	GENIC	homozygous	143823199
2	44843801	44843801		GAAA	38	GENIC	homozygous	143814542
2	44843802	44843802		TCTTATGT	38	GENIC	homozygous	143814543
2	44846666	44846666		T	31	GENIC	homozygous	135903802
2	44846678	44846679	T	C	29	GENIC	homozygous	136092109
2	44847320	44847321	T	C	52	GENIC	homozygous	136092110
2	44847593	44847594	T	C	41	GENIC	homozygous	143823200
2	44848053	44848053		A	41	GENIC	homozygous	143814544
2	44848218	44848219	A	G	30	GENIC	homozygous	143823201
2	44848229	44848230	C	T	29	GENIC	homozygous	136092111
2	44848668	44848668		AGGTAAG	39	GENIC	homozygous	141323126