chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	97736059	97736060	G	T	24	GENIC	homozygous	117181026
10	97737114	97737115	A	G	35	GENIC	possibly homozygous	116694623
10	97737956	97737957	C	T	24	GENIC	homozygous	117181027
10	97739165	97739166	A	G	14	GENIC	homozygous	117023699
10	97739874	97739875	A	G	11	GENIC	homozygous	116694637
10	97741450	97741451	A	G	16	GENIC	possibly homozygous	116694645
10	97741631	97741632	C	T	24	GENIC	possibly homozygous	117181028
10	97743444	97743445	T	C	26	GENIC	possibly homozygous	117181029
10	97743596	97743597	C	T	25	GENIC	possibly homozygous	116694657
10	97745288	97745289	T	C	26	GENIC	homozygous	117023708
10	97745657	97745658	G	A	31	GENIC	homozygous	117181030
10	97746053	97746054	C	T	20	GENIC	homozygous	117181031
10	97746838	97746839	A	G	33	GENIC	homozygous	116694661
10	97748798	97748799	A	G	17	GENIC	possibly homozygous	117181032
10	97748820	97748821	C	A	15	GENIC	homozygous	117181033
10	97751159	97751160	G	A	34	GENIC	possibly homozygous	117181034
10	97751625	97751626	C	T	25	GENIC	homozygous	117181035
10	97754389	97754390	G	A	22	GENIC	homozygous	116694679
10	97754437	97754438	G	A	14	GENIC	homozygous	116694681
10	97755820	97755821	G	A	31	GENIC	homozygous	117181036
10	97755967	97755968	T	C	16	GENIC	homozygous	116694685
10	97757698	97757699	G	A	9	GENIC	homozygous	116694691
10	97758531	97758532	T	A	31	GENIC	possibly homozygous	116694693