chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	251331177	251331178	C	T	47	GENIC	possibly homozygous	108610018
1	251331194	251331195	T	A	45	GENIC	possibly homozygous	108610019
1	251331235	251331236	T	C	32	GENIC	heterozygous	108610020
1	251331258	251331259	G	A	33	GENIC	heterozygous	108610021
1	251331288	251331289	T	C	34	GENIC	heterozygous	108779593
1	251331312	251331313	G	A	31	GENIC	heterozygous	109019415
1	251331317	251331318	A	G	33	GENIC	heterozygous	109019416
1	251331340	251331341	G	A	33	GENIC	heterozygous	109019417
1	251331343	251331344	C	A	32	GENIC	heterozygous	109019418
1	251332991	251332992	A	G	34	GENIC	heterozygous	109019423
1	251332999	251333000	A	C	38	GENIC	heterozygous	109019424
1	251333016	251333017	G	T	38	GENIC	heterozygous	108779595
1	251333040	251333041	T	A	38	GENIC	heterozygous	108610022
1	251333045	251333046	A	C	32	GENIC	heterozygous	108610023
1	251333050	251333051	T	C	35	GENIC	heterozygous	108610024
1	251333071	251333072	T	C	35	GENIC	heterozygous	108610025
1	251333072	251333073	G	A	34	GENIC	heterozygous	108610026
1	251333088	251333089	A	C	43	GENIC	heterozygous	108610027
1	251333109	251333110	G	T	36	GENIC	heterozygous	108610028
1	251333118	251333119	C	T	42	GENIC	heterozygous	108610029
1	251333125	251333126	T	C	45	GENIC	heterozygous	108610030
1	251333134	251333135	T	A	41	GENIC	possibly homozygous	108610031
1	251333143	251333144	T	C	41	GENIC	possibly homozygous	108610032