chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	82596079	82596080	G	T	29	GENIC	homozygous	108878302
1	82596530	82596531	T	C	15	GENIC	homozygous	108878304
1	82596562	82596563	G	A	18	GENIC	homozygous	120482030
1	82596899	82596900	A	T	18	GENIC	homozygous	120482031
1	82597757	82597758	T	C	8	GENIC	homozygous	108878307
1	82599475	82599476	C	T	5	GENIC	homozygous	120820220
1	82599893	82599894	A	G	30	GENIC	homozygous	108878311
1	82600292	82600293	T	C	33	GENIC	homozygous	108878312
1	82600641	82600642	T	C	26	GENIC	homozygous	108878313
1	82600686	82600687	T	C	19	GENIC	homozygous	108878314
1	82600708	82600709	C	G	19	GENIC	homozygous	109302610
1	82601527	82601528	T	C	19	GENIC	homozygous	120482033
1	82601594	82601595	A	G	22	GENIC	homozygous	108878315
1	82601993	82601994	A	T	12	GENIC	homozygous	108140575
1	82603827	82603828	A	G	29	GENIC	homozygous	108878316
1	82604268	82604269	A	C	18	GENIC	homozygous	109302620
1	82604364	82604365	G	A	19	GENIC	homozygous	120482034
1	82604807	82604808	T	C	3	GENIC	homozygous	120820221
1	82605105	82605106	G	A	21	GENIC	homozygous	108878318
1	82605239	82605240	T	C	17	GENIC	homozygous	108878319
1	82605630	82605631	A	G	26	GENIC	homozygous	109561154
1	82606266	82606267	C	T	23	GENIC	homozygous	108878323
1	82606721	82606722	T	A	10	GENIC	homozygous	108878325
1	82606771	82606772	G	A	17	GENIC	homozygous	108878326
1	82609964	82609965	T	C	14	GENIC	homozygous	108140580
1	82608524	82608525	T	C	20	GENIC	homozygous	108878329
1	82608964	82608965	C	T	16	GENIC	homozygous	120482035
1	82608977	82608978	C	T	17	GENIC	homozygous	108878330