chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	80323339	80323340	T	G	49	GENIC	homozygous	142835330
1	80323976	80323977	G	T	48	GENIC	homozygous	142835331
1	80324058	80324059	T	G	44	GENIC	homozygous	142835332
1	80325245	80325246	A	G	41	GENIC	homozygous	142835333
1	80325300	80325301	T	C	39	GENIC	homozygous	142835334
1	80325538	80325539	T	G	53	GENIC	homozygous	142835335
1	80325546	80325547	C	T	51	GENIC	homozygous	142835336
1	80326523	80326524	T	C	46	GENIC	homozygous	142835337
1	80327080	80327081	T	G	51	GENIC	heterozygous	142835338
1	80327081	80327082	G	A	50	GENIC	heterozygous	142835339
1	80327385	80327386	A	G	33	GENIC	heterozygous	142835340
1	80327389	80327390	T	C	33	GENIC	heterozygous	142835341
1	80327800	80327801	G	T	43	GENIC	homozygous	142835342
1	80327802	80327803	C	T	42	GENIC	homozygous	142835343
1	80327824	80327825	G	T	40	GENIC	homozygous	142835344
1	80327837	80327838	A	G	35	GENIC	homozygous	142835345
1	80327864	80327865	T	A	36	GENIC	homozygous	142835346
1	80327610	80327611	A		43	GENIC	heterozygous	145234033
1	80325633	80325637	CCCT		38	GENIC	homozygous	142788749
1	80327610	80327611	A	G	43	GENIC	homozygous	153861126
1	80327916	80327917	C	T	37	GENIC	homozygous	142835347
1	80327918	80327919	T	C	37	GENIC	homozygous	142835348
1	80327949	80327950	A	G	41	GENIC	homozygous	142835349