chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	97979500	97979501	T	C	16	GENIC	homozygous	58975722
2	97979745	97979746	G	T	26	GENIC	homozygous	61724060
2	97980110	97980111	G	-	21	GENIC	homozygous	61724062
2	97980578	97980579	C	T	27	GENIC	homozygous	58975723
2	97980720	97980721	A	C	26	GENIC	homozygous	60448388
2	97980721	97980722	C	A	26	GENIC	homozygous	60448389
2	97981534	97981535	C	T	17	GENIC	homozygous	61349681
2	97981599	97981600	G	C	23	GENIC	homozygous	58975724
2	97981702	97981703	T	C	36	GENIC	homozygous	58975725
2	97981911	97981912	C	T	23	GENIC	homozygous	61724064
2	97982033	97982034	G	A	11	GENIC	homozygous	61724066
2	97982081	97982082	T	-	5	GENIC	homozygous	58975727
2	97983852	97983853	C	T	16	GENIC	homozygous	58975738
2	97983983	97983984	G	C	13	GENIC	homozygous	58975741
2	97985305	97985306	C	T	25	GENIC	possibly homozygous	58975748
2	97985589	97985590	C	T	23	GENIC	homozygous	58975749
2	97985627	97985628	C	-	30	GENIC	homozygous	61724069
2	97985628	97985629	C	T	31	GENIC	homozygous	61724071
2	97986919	97986920	G	A	21	GENIC	homozygous	61724073
2	97987209	97987210	T	C	18	GENIC	homozygous	58975751
2	97987847	97987848	G	A	26	GENIC	homozygous	61724075
2	97987998	97987999	T	C	24	GENIC	homozygous	58975754
2	97988658	97988659	A	G	26	GENIC	homozygous	58975755
2	97989005	97989006	T	-	16	GENIC	homozygous	58975757
2	97989081	97989082	T	C	24	GENIC	homozygous	58975758
2	97989084	97989085	A	G	25	GENIC	homozygous	58975759
2	97989323	97989324	A	C	24	GENIC	possibly homozygous	58975760
2	97989563	97989564	C	T	26	GENIC	homozygous	58975761
2	97989663	97989664	A	-	24	GENIC	homozygous	61724077
2	97989665	97989666	T	TC	24	GENIC	homozygous	61724079
2	97989818	97989819	T	C	18	GENIC	homozygous	58975762
2	97990481	97990482	G	C	24	GENIC	possibly homozygous	61724081
2	97990535	97990536	C	T	17	GENIC	homozygous	61724083
2	97991110	97991111	A	G	29	GENIC	possibly homozygous	61724085
2	97991870	97991871	T	TTC	1	GENIC	homozygous	62169847