chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	41137798	41137799	A	C	11	GENIC	homozygous	60442786
2	41137984	41137985	T	C	19	GENIC	homozygous	60442787
2	41138056	41138057	G	A	13	GENIC	homozygous	60442788
2	41138081	41138082	T	G	14	GENIC	homozygous	60476882
2	41138082	41138083	A	G	15	GENIC	homozygous	60476883
2	41138097	41138098	C	G	17	GENIC	homozygous	60476884
2	41138099	41138100	T	A	16	GENIC	homozygous	60442789
2	41138175	41138176	A	C	15	GENIC	homozygous	60442790
2	41138181	41138182	C	G	14	GENIC	homozygous	60442791
2	41138189	41138190	A	AC	9	GENIC	homozygous	60442792
2	41138192	41138193	T	C	12	GENIC	homozygous	60442793
2	41138638	41138639	A	T	35	GENIC	homozygous	60442794
2	41138645	41138646	A	-	39	GENIC	homozygous	58778872
2	41138200	41138201	T	C	16	GENIC	homozygous	58778866
2	41140627	41140628	A	G	15	GENIC	homozygous	58778888
2	41141998	41141999	A	G	29	GENIC	homozygous	58778916
2	41142098	41142099	T	C	25	GENIC	homozygous	58778920
2	41142449	41142450	A	C	34	GENIC	homozygous	58778936
2	41142850	41142851	T	TGTTTG	6	GENIC	heterozygous	60476885
2	41143505	41143506	A	G	35	GENIC	homozygous	58778960
2	41143954	41143955	C	-	9	GENIC	possibly homozygous	58778966
2	41144358	41144360	AT	--	30	GENIC	homozygous	60442795
2	41146912	41146913	A	G	31	GENIC	homozygous	58778984
2	41147137	41147138	C	T	37	GENIC	homozygous	60442796
2	41147720	41147721	T	C	31	GENIC	homozygous	58778990