chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	80171042	80171042		A	45	GENIC	possibly homozygous	131258302
1	80171186	80171187	G	A	45	GENIC	homozygous	109298332
1	80171941	80171942	A	T	38	GENIC	homozygous	109298334
1	80172032	80172033	T	C	47	GENIC	homozygous	109298336
1	80174003	80174004	C	T	41	GENIC	homozygous	109298338
1	80174219	80174220	A	C	31	GENIC	homozygous	109298340
1	80174431	80174432	A	C	38	GENIC	homozygous	109298344
1	80175820	80175821	T	C	40	GENIC	homozygous	109298347
1	80175908	80175909	T	A	49	GENIC	homozygous	109298349
1	80176774	80176775	T	C	35	GENIC	homozygous	109298351
1	80177439	80177440	A	G	28	GENIC	homozygous	109298353
1	80177997	80178001	CTGT		39	GENIC	homozygous	131258303
1	80180735	80180736	A	T	38	GENIC	homozygous	109298355
1	80180801	80180802	C	T	46	GENIC	homozygous	109298357
1	80181181	80181182	T	C	42	GENIC	homozygous	109298359
1	80182014	80182015	G	A	40	GENIC	homozygous	109298361
1	80182425	80182426	A	G	40	GENIC	homozygous	109298363
1	80183136	80183137	A	G	55	GENIC	possibly homozygous	109298367
1	80185863	80185864	C	G	40	GENIC	homozygous	109298369
1	80185455	80185456	C	A	43	GENIC	homozygous	120868283
1	80176978	80176978		GGGA	9	GENIC	homozygous	131575746
1	80185017	80185017		CCG	27	GENIC	homozygous	127397505