chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	98562986	98562987	G	A	50	GENIC	homozygous	109315660
1	98563579	98563580	C	T	37	GENIC	possibly homozygous	108161508
1	98563583	98563584	T	G	36	GENIC	possibly homozygous	108161509
1	98564794	98564795	C	T	40	GENIC	homozygous	109315662
1	98564971	98564972	G	C	59	GENIC	homozygous	108161510
1	98566458	98566459	T	G	38	GENIC	homozygous	108161515
1	98568219	98568220	A	G	44	GENIC	homozygous	108161516
1	98566469	98566470	G		31	GENIC	homozygous	127407715
1	98565496	98565496		T	55	GENIC	possibly homozygous	131577414
1	98569664	98569664		TT	35	GENIC	homozygous	131577415
1	98569684	98569685	C	T	34	GENIC	homozygous	108896688
1	98569884	98569885	C	G	45	GENIC	possibly homozygous	108896689
1	98570205	98570206	A	C	35	GENIC	homozygous	108896690
1	98570208	98570209	C	G	37	GENIC	homozygous	108896691
1	98570210	98570211	A	C	39	GENIC	homozygous	108896692
1	98570214	98570215	C	T	39	GENIC	homozygous	108896693
1	98570413	98570414	C	T	41	GENIC	homozygous	120514391
1	98570415	98570416	T	C	41	GENIC	homozygous	120514392
1	98570498	98570499	C	T	37	GENIC	homozygous	108161519
1	98570970	98570971	C	T	47	GENIC	homozygous	109315664
1	98570983	98570984	G	A	47	GENIC	homozygous	109315666