chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	82596079	82596080	G	T	47	GENIC	homozygous	108878302
1	82596134	82596135	G	A	41	GENIC	homozygous	108878303
1	82596530	82596531	T	C	28	GENIC	homozygous	108878304
1	82597757	82597758	T	C	21	GENIC	homozygous	108878307
1	82599401	82599402	T	C	32	GENIC	homozygous	108878310
1	82599893	82599894	A	G	28	GENIC	homozygous	108878311
1	82600292	82600293	T	C	30	GENIC	homozygous	108878312
1	82600641	82600642	T	C	48	GENIC	possibly homozygous	108878313
1	82600686	82600687	T	C	41	GENIC	possibly homozygous	108878314
1	82600708	82600709	C	G	30	GENIC	possibly homozygous	109302610
1	82600852	82600853	T	C	46	GENIC	homozygous	109302612
1	82601594	82601595	A	G	40	GENIC	homozygous	108878315
1	82601993	82601994	A	T	26	GENIC	homozygous	108140575
1	82602794	82602795	A	G	27	GENIC	homozygous	109302618
1	82603827	82603828	A	G	31	GENIC	homozygous	108878316
1	82604268	82604269	A	C	32	GENIC	homozygous	109302620
1	82605105	82605106	G	A	18	GENIC	homozygous	108878318
1	82605239	82605240	T	C	22	GENIC	homozygous	108878319
1	82606266	82606267	C	T	19	GENIC	homozygous	108878323
1	82606721	82606722	T	A	14	GENIC	homozygous	108878325
1	82606771	82606772	G	A	24	GENIC	homozygous	108878326
1	82608524	82608525	T	C	41	GENIC	homozygous	108878329
1	82608977	82608978	C	T	28	GENIC	homozygous	108878330
1	82609964	82609965	T	C	31	GENIC	homozygous	108140580