chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	140756299	140756300	C	A	9	GENIC	homozygous	61901740
1	140756458	140756459	A	T	13	GENIC	heterozygous	61901741
1	140756502	140756503	G	A	14	GENIC	homozygous	61901742
1	140756738	140756739	C	G	3	GENIC	homozygous	61901743
1	140756742	140756743	T	C	4	GENIC	heterozygous	61901744
1	140757180	140757181	A	-	6	GENIC	heterozygous	60871250
1	140757351	140757352	G	A	13	GENIC	possibly homozygous	61901745
1	140757409	140757410	G	A	5	GENIC	heterozygous	61901746
1	140757487	140757488	T	G	11	GENIC	homozygous	61901747
1	140757549	140757550	A	T	12	GENIC	homozygous	61901748
1	140757615	140757616	T	C	15	GENIC	homozygous	61901749
1	140757729	140757730	C	T	7	GENIC	possibly homozygous	61901750
1	140757735	140757736	C	T	5	GENIC	heterozygous	61901751
1	140758451	140758452	T	A	12	GENIC	homozygous	61901752
1	140758794	140758795	T	C	9	GENIC	homozygous	61901753
1	140758860	140758861	C	CA	10	GENIC	homozygous	61901754
1	140759215	140759216	T	C	9	GENIC	heterozygous	61901755
1	140759762	140759763	C	T	18	GENIC	possibly homozygous	61901757
1	140759973	140759974	T	C	13	GENIC	homozygous	60871251
1	140759993	140759994	G	T	9	GENIC	homozygous	61901758
1	140760129	140760130	A	G	18	GENIC	homozygous	61901759
1	140760294	140760295	A	G	19	GENIC	possibly homozygous	60871252
1	140760428	140760429	G	A	9	GENIC	homozygous	62160989
1	140760430	140760431	A	G	10	GENIC	homozygous	62160991
1	140760698	140760699	C	T	10	GENIC	possibly homozygous	61901760
1	140760828	140760829	G	A	19	GENIC	possibly homozygous	61901761
1	140760919	140760920	C	A	11	GENIC	homozygous	61901762
1	140760987	140760988	G	C	8	GENIC	homozygous	61901763
1	140761272	140761273	T	TA	7	GENIC	homozygous	61901764
1	140761329	140761330	T	C	9	GENIC	homozygous	61901765
1	140761449	140761450	G	A	12	GENIC	possibly homozygous	61901766
1	140761482	140761483	G	A	13	GENIC	homozygous	61901767
1	140761833	140761834	C	A	13	GENIC	homozygous	61901768