chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	102900388	102900389	C	G	19	GENIC	homozygous	109115303
1	102901884	102901886	TG		14	GENIC	homozygous	130818462
1	102902990	102902991	A	G	18	GENIC	homozygous	109115305
1	102903115	102903115		T	10	GENIC	homozygous	130818463
1	102904457	102904458	G	A	18	GENIC	homozygous	109115307
1	102905859	102905860	C	T	22	GENIC	homozygous	109115309
1	102906236	102906237	T	C	20	GENIC	homozygous	109115311
1	102906280	102906281	C	A	19	GENIC	homozygous	109115313
1	102906321	102906322	T	C	19	GENIC	homozygous	109115315
1	102906857	102906858	T	G	11	GENIC	homozygous	109115317
1	102906861	102906862	A	C	12	GENIC	homozygous	109115319
1	102906877	102906878	T		12	GENIC	homozygous	130818464
1	102906990	102906991	A	G	16	GENIC	homozygous	109115321
1	102907239	102907240	C	T	9	GENIC	homozygous	109115323
1	102907754	102907755	G	A	13	GENIC	homozygous	109115325
1	102908286	102908287	A	T	13	GENIC	homozygous	109115327
1	102908597	102908598	A	G	17	GENIC	homozygous	109115329
1	102909001	102909004	AGG		9	GENIC	homozygous	130818465
1	102909621	102909622	T	C	23	GENIC	possibly homozygous	109115335