chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	84019314	84019315	C	T	29	GENIC	possibly homozygous	108879875
1	84019577	84019578	G	A	29	GENIC	possibly homozygous	108879876
1	84019635	84019636	G	A	19	GENIC	possibly homozygous	108879877
1	84019852	84019853	C	T	29	GENIC	possibly homozygous	108879878
1	84021085	84021086	G	A	13	GENIC	homozygous	108879879
1	84021538	84021539	A	G	23	GENIC	possibly homozygous	108879885
1	84022178	84022179	A	T	20	GENIC	homozygous	108879886
1	84022180	84022181	G	A	21	GENIC	homozygous	108879887
1	84023378	84023379	A	G	23	GENIC	homozygous	108879889
1	84023593	84023594	G	A	24	GENIC	possibly homozygous	108879890
1	84024233	84024234	A	C	19	GENIC	possibly homozygous	108879891
1	84025225	84025226	G	T	28	GENIC	homozygous	108879892
1	84026255	84026256	T	C	8	GENIC	homozygous	108879893
1	84026566	84026567	A	G	22	GENIC	possibly homozygous	108879894
1	84026762	84026763	C	A	32	GENIC	possibly homozygous	108879895
1	84027093	84027094	A	G	18	GENIC	homozygous	108879896
1	84027503	84027504	G	A	23	GENIC	homozygous	108879897
1	84028150	84028151	T	A	24	GENIC	possibly homozygous	108879898
1	84031115	84031116	A	G	33	GENIC	possibly homozygous	108879900
1	84031130	84031131	T	G	33	GENIC	possibly homozygous	108879901
1	84031898	84031899	A	T	26	GENIC	possibly homozygous	108879902
1	84033481	84033482	T	C	26	GENIC	heterozygous	108879904
1	84034450	84034451	A	G	20	GENIC	homozygous	108879906
1	84034913	84034914	A	G	22	GENIC	possibly homozygous	108879907
1	84035025	84035026	T	C	24	GENIC	homozygous	108879908
1	84036487	84036488	T	G	16	GENIC	possibly homozygous	108879909
1	84036935	84036936	A	G	25	GENIC	possibly homozygous	108879910
1	84038230	84038231	A	T	18	GENIC	homozygous	108879912
1	84038414	84038415	A	G	21	GENIC	homozygous	108879913
1	84040201	84040202	G	A	15	GENIC	homozygous	120667207