chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	238417427	238417428	G	T	61	GENIC	homozygous	108581995
1	238455670	238455671	C	G	2	GENIC	homozygous	109205809
1	238455790	238455791	A	G	27	GENIC	possibly homozygous	108582187
1	238455834	238455835	A	G	18	GENIC	homozygous	108582189
1	238455837	238455838	C	A	18	GENIC	homozygous	108582191
1	238455845	238455846	C	G	18	GENIC	homozygous	108582193
1	238471909	238471910	C	T	52	GENIC	heterozygous	109205811
1	238478728	238478729	T	A	37	GENIC	possibly homozygous	108582311
1	238488144	238488145	T	A	56	GENIC	homozygous	108582345
1	238491133	238491134	G	A	21	GENIC	heterozygous	108582349
1	238507353	238507354	A	T	136	GENIC	heterozygous	108582351
1	238510138	238510139	T	C	32	GENIC	possibly homozygous	108773586
1	238510599	238510600	T	A	41	GENIC	heterozygous	108582353
1	238510630	238510631	C	T	94	GENIC	heterozygous	109205813
1	238511297	238511298	G	T	76	GENIC	heterozygous	109205815
1	238511316	238511317	A	C	52	GENIC	heterozygous	109205817
1	238511324	238511325	T	C	48	GENIC	heterozygous	109057467
1	238511523	238511524	G	C	52	GENIC	heterozygous	108582361
1	238511651	238511652	T	G	44	GENIC	possibly homozygous	108582363
1	238511712	238511713	T	C	28	GENIC	possibly homozygous	108582365
1	238511819	238511820	T	G	45	GENIC	heterozygous	108582367
1	238523773	238523774	G	A	24	GENIC	homozygous	108582375
1	238524693	238524694	T	A	32	GENIC	homozygous	108773591
1	238524694	238524695	T	A	32	GENIC	homozygous	108773592
1	238524773	238524774	C	A	38	GENIC	homozygous	108582377
1	238524779	238524780	C	A	26	GENIC	homozygous	108582379
1	238524811	238524812	C	A	39	GENIC	homozygous	108582381
1	238525002	238525003	C	A	17	GENIC	homozygous	108582383
1	238525143	238525144	G	T	33	GENIC	possibly homozygous	108582385
1	238525518	238525519	T	C	41	GENIC	possibly homozygous	108582387
1	238525571	238525572	C	G	49	GENIC	homozygous	108582389