chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	265434406	265434407	T	G	1	GENIC	homozygous	61194234
1	265435693	265435694	T	C	2	GENIC	homozygous	61194240
1	265435696	265435697	C	A	2	GENIC	heterozygous	61194242
1	265435923	265435924	G	A	5	GENIC	heterozygous	61194244
1	265436393	265436394	A	G	8	GENIC	homozygous	61194246
1	265436394	265436395	T	TG	2	GENIC	homozygous	61194248
1	265436506	265436507	T	C	13	GENIC	homozygous	61194252
1	265437194	265437195	A	ATCT	9	GENIC	homozygous	61194258
1	265437709	265437710	T	A	11	GENIC	homozygous	61194260
1	265438573	265438574	A	G	1	GENIC	homozygous	61194262
1	265440062	265440063	G	GC	9	GENIC	heterozygous	62112064
1	265443585	265443586	C	G	3	GENIC	homozygous	61194292
1	265443589	265443590	A	G	2	GENIC	homozygous	61194294
1	265444734	265444735	C	G	16	GENIC	homozygous	61194297
1	265446045	265446046	T	C	4	GENIC	heterozygous	61194301
1	265446621	265446622	T	C	1	GENIC	homozygous	61194303
1	265447184	265447188	CCCC	----	4	GENIC	heterozygous	61194305
1	265448505	265448506	T	C	13	GENIC	homozygous	61194307
1	265449424	265449425	A	G	8	GENIC	possibly homozygous	61194309
1	265450496	265450497	A	G	24	GENIC	possibly homozygous	61194311
1	265451897	265451898	T	C	17	GENIC	homozygous	61194312
1	265453399	265453400	A	T	10	GENIC	possibly homozygous	61194314