chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	280097143	280097144	C	T	42	GENIC	homozygous	108811071
1	280097247	280097248	A	C	47	GENIC	homozygous	108811073
1	280099463	280099464	G	A	37	GENIC	homozygous	108666484
1	280101968	280101969	T	G	30	GENIC	homozygous	108811075
1	280102670	280102671	T	G	37	GENIC	possibly homozygous	108811077
1	280102938	280102939	G	A	41	GENIC	homozygous	108811079
1	280103577	280103578	C	T	34	GENIC	homozygous	108811081
1	280104940	280104941	A	G	41	GENIC	homozygous	109222275
1	280105611	280105612	G	T	39	GENIC	homozygous	109222277
1	280106071	280106072	C	T	29	GENIC	homozygous	109222279
1	280107947	280107948	G	C	50	GENIC	homozygous	109222281
1	280109000	280109001	C	T	54	GENIC	homozygous	109222283
1	280109196	280109197	G	T	36	GENIC	homozygous	109222285
1	280111519	280111520	C	T	45	GENIC	homozygous	109222287
1	280111721	280111722	A	T	31	GENIC	homozygous	109222289
1	280114394	280114395	T	C	20	GENIC	homozygous	109222291
1	280115287	280115288	A	G	35	GENIC	homozygous	108666488
1	280115463	280115464	T	C	35	GENIC	homozygous	109222293
1	280116701	280116702	A	G	38	GENIC	homozygous	108666490
1	280119493	280119494	T	C	34	GENIC	homozygous	108666492
1	280120568	280120569	G	A	49	GENIC	homozygous	108811088
1	280120856	280120857	C	T	43	GENIC	homozygous	109222295
1	280121671	280121672	T	C	26	GENIC	possibly homozygous	109222297
1	280122083	280122084	C	T	25	GENIC	homozygous	109222299
1	280122235	280122236	A	G	40	GENIC	possibly homozygous	109222301
1	280123084	280123085	A	C	23	GENIC	heterozygous	109222303
1	280123090	280123091	G	A	23	GENIC	heterozygous	109222305
1	280123091	280123092	C	T	24	GENIC	heterozygous	109222307
1	280123101	280123102	C	A	25	GENIC	heterozygous	109222309
1	280123125	280123126	T	C	21	GENIC	heterozygous	109222311
1	280125751	280125752	C	T	40	GENIC	homozygous	109222313
1	280126709	280126710	A	C	35	GENIC	homozygous	108666494
1	280127299	280127300	C	A	36	GENIC	homozygous	109222315
1	280127771	280127772	T	C	37	GENIC	homozygous	108666497