chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	82596079	82596080	G	T	18	GENIC	homozygous	108878302
1	82596134	82596135	G	A	24	GENIC	homozygous	108878303
1	82596530	82596531	T	C	17	GENIC	homozygous	108878304
1	82598062	82598063	T	C	24	GENIC	homozygous	108878308
1	82599112	82599113	G	A	19	GENIC	homozygous	108878309
1	82599893	82599894	A	G	23	GENIC	homozygous	108878311
1	82600292	82600293	T	C	11	GENIC	homozygous	108878312
1	82600641	82600642	T	C	20	GENIC	homozygous	108878313
1	82600686	82600687	T	C	21	GENIC	homozygous	108878314
1	82601594	82601595	A	G	19	GENIC	homozygous	108878315
1	82603827	82603828	A	G	23	GENIC	homozygous	108878316
1	82604247	82604248	C	T	14	GENIC	homozygous	108878317
1	82605105	82605106	G	A	19	GENIC	homozygous	108878318
1	82605239	82605240	T	C	21	GENIC	homozygous	108878319
1	82605461	82605462	C	T	21	GENIC	homozygous	108878320
1	82605693	82605694	G	A	23	GENIC	homozygous	108878321
1	82606266	82606267	C	T	19	GENIC	homozygous	108878323
1	82606721	82606722	T	A	7	GENIC	homozygous	108878325
1	82606771	82606772	G	A	16	GENIC	homozygous	108878326
1	82607385	82607386	C	G	26	GENIC	homozygous	108878327
1	82607947	82607948	C	T	22	GENIC	homozygous	108878328
1	82608524	82608525	T	C	15	GENIC	homozygous	108878329
1	82608977	82608978	C	T	20	GENIC	homozygous	108878330