chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	250094826	250094827	A	G	59	GENIC	homozygous	108607491
1	250095810	250095811	T	C	52	GENIC	homozygous	108607492
1	250095818	250095819	C	T	54	GENIC	homozygous	108607493
1	250096019	250096020	T	C	67	GENIC	homozygous	108607494
1	250096043	250096044	A	G	68	GENIC	homozygous	108607495
1	250096171	250096172	C	G	51	GENIC	homozygous	108607496
1	250096244	250096245	T	C	63	GENIC	homozygous	108607497
1	250096650	250096651	A	G	84	GENIC	homozygous	108607498
1	250096986	250096987	C	T	94	GENIC	homozygous	108607499
1	250097178	250097179	C	T	66	GENIC	possibly homozygous	108607500
1	250097429	250097430	C	T	51	GENIC	homozygous	108607501
1	250097864	250097865	A	C	63	GENIC	possibly homozygous	108607502
1	250100166	250100167	T	C	62	GENIC	homozygous	108607503
1	250100349	250100350	A	C	95	GENIC	homozygous	108607504
1	250100470	250100471	C	T	68	GENIC	homozygous	108607505
1	250100607	250100608	C	A	77	GENIC	possibly homozygous	108607506
1	250100801	250100802	G	A	63	GENIC	homozygous	108607507
1	250100988	250100989	A	G	78	GENIC	homozygous	108607508
1	250101222	250101223	T	G	89	GENIC	possibly homozygous	108607509