chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	44840970	44840971	T	C	18	GENIC	homozygous	136092101
2	44841305	44841306	T	C	16	GENIC	homozygous	136092102
2	44841547	44841548	C	T	15	GENIC	homozygous	136092103
2	44843004	44843005	T	C	20	GENIC	homozygous	136092104
2	44843275	44843275		CCATTGCGT	15	GENIC	homozygous	135903797
2	44843551	44843552	A	T	14	GENIC	homozygous	136092105
2	44843675	44843676	A		9	GENIC	homozygous	135903798
2	44843813	44843814	A	G	14	GENIC	homozygous	136092106
2	44844313	44844313		AGAT	20	GENIC	homozygous	135903799
2	44844388	44844389	A	G	29	GENIC	homozygous	136092107
2	44844570	44844571	C	T	19	GENIC	homozygous	136092108
2	44846529	44846532	CAC		12	GENIC	homozygous	135903800
2	44846548	44846566	ATCATCATCATCATCATG		12	GENIC	homozygous	135903801
2	44846666	44846666		T	16	GENIC	homozygous	135903802
2	44846678	44846679	T	C	17	GENIC	homozygous	136092109
2	44847320	44847321	T	C	12	GENIC	homozygous	136092110
2	44848229	44848230	C	T	9	GENIC	homozygous	136092111
2	44848671	44848671		TAA	19	GENIC	homozygous	135903803
2	44848672	44848672		AGGA	20	GENIC	homozygous	135903804