chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	86397126	86397134	TTTATTTA		9	GENIC	homozygous	128841980
10	86397136	86397137	T	G	10	GENIC	homozygous	116667550
10	86397422	86397423	C	T	18	GENIC	homozygous	116816175
10	86398731	86398732	A	C	13	GENIC	homozygous	116667552
10	86398897	86398898	T	C	21	GENIC	homozygous	116667554
10	86399258	86399259	A	G	12	GENIC	homozygous	116667556
10	86399304	86399304		GG	9	GENIC	homozygous	128841981
10	86400606	86400607	C	T	6	GENIC	homozygous	116816179
10	86400815	86400816	T	A	17	GENIC	homozygous	116667558
10	86401011	86401012	G	T	14	GENIC	homozygous	116667560
10	86401096	86401097	A	T	22	GENIC	homozygous	116816181
10	86401469	86401470	G	C	17	GENIC	homozygous	116816183
10	86402476	86402477	G	C	14	GENIC	homozygous	116816189
10	86402787	86402788	A	G	21	GENIC	homozygous	116816193
10	86404073	86404074	G	A	25	GENIC	homozygous	117019370
10	86398961	86398962	T	C	24	GENIC	homozygous	117258398
10	86399194	86399195	T	G	11	GENIC	homozygous	117258400
10	86401843	86401844	G	A	22	GENIC	homozygous	117019364
10	86402032	86402033	C	G	10	GENIC	homozygous	117019365
10	86402200	86402201	T	C	17	GENIC	homozygous	117019366
10	86403261	86403262	C	T	21	GENIC	homozygous	117019367
10	86403791	86403792	G	C	14	GENIC	homozygous	117019368
10	86404061	86404062	T	A	27	GENIC	possibly homozygous	117019369
10	86405981	86405982	C	T	12	GENIC	heterozygous	133681716
10	86406632	86406633	C	G	18	GENIC	homozygous	117019371
10	86406894	86406895	T	C	15	GENIC	homozygous	116667576
10	86407659	86407660	G	T	15	GENIC	homozygous	116667578