chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	97979500	97979501	T	C	27	GENIC	homozygous	58975722
2	97980578	97980579	C	T	33	GENIC	homozygous	58975723
2	97980720	97980721	A	C	29	GENIC	homozygous	60448388
2	97980721	97980722	C	A	29	GENIC	homozygous	60448389
2	97981599	97981600	G	C	28	GENIC	homozygous	58975724
2	97981702	97981703	T	C	29	GENIC	homozygous	58975725
2	97982081	97982082	T	-	8	GENIC	possibly homozygous	58975727
2	97983628	97983629	G	A	16	GENIC	homozygous	58975737
2	97983852	97983853	C	T	13	GENIC	homozygous	58975738
2	97983909	97983910	A	G	9	GENIC	homozygous	58975739
2	97983939	97983940	G	-	12	GENIC	homozygous	58975740
2	97983983	97983984	G	C	11	GENIC	homozygous	58975741
2	97984022	97984023	C	A	8	GENIC	homozygous	58975742
2	97984073	97984079	CCCCCT	------	7	GENIC	homozygous	58975743
2	97984224	97984225	G	A	13	GENIC	homozygous	58975744
2	97984675	97984676	C	A	27	GENIC	homozygous	58975745
2	97984697	97984698	A	C	23	GENIC	homozygous	58975746
2	97984744	97984745	T	A	25	GENIC	homozygous	58975747
2	97985305	97985306	C	T	36	GENIC	homozygous	58975748
2	97985589	97985590	C	T	32	GENIC	homozygous	58975749
2	97985883	97985884	C	T	34	GENIC	homozygous	58975750
2	97987209	97987210	T	C	48	GENIC	homozygous	58975751
2	97987613	97987614	C	T	29	GENIC	homozygous	58975752
2	97987842	97987847	GTTGC	-----	40	GENIC	homozygous	58975753
2	97987998	97987999	T	C	23	GENIC	homozygous	58975754
2	97988658	97988659	A	G	26	GENIC	homozygous	58975755
2	97988902	97988915	AAAAAAAAAAAAA	-------------	17	GENIC	possibly homozygous	58975756
2	97989005	97989006	T	-	11	GENIC	homozygous	58975757
2	97989081	97989082	T	C	31	GENIC	homozygous	58975758
2	97989084	97989085	A	G	32	GENIC	homozygous	58975759
2	97989323	97989324	A	C	20	GENIC	homozygous	58975760
2	97989563	97989564	C	T	36	GENIC	homozygous	58975761
2	97989818	97989819	T	C	25	GENIC	homozygous	58975762
2	97990393	97990403	ATTTTCCCTT	----------	15	GENIC	homozygous	58975763
2	97990681	97990682	A	G	27	GENIC	homozygous	58975764