chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	91164886	91164887	A	G	21	GENIC	homozygous	116821803
10	91167489	91167490	G	A	39	GENIC	possibly homozygous	116905469
10	91167931	91167932	C	T	30	GENIC	possibly homozygous	116905471
10	91169530	91169531	G	A	20	GENIC	possibly homozygous	116905475
10	91169645	91169646	G	A	36	GENIC	homozygous	116905477
10	91169674	91169675	G	A	45	GENIC	homozygous	116905479
10	91170142	91170143	A	G	24	GENIC	possibly homozygous	116905481
10	91170377	91170378	C	T	27	GENIC	possibly homozygous	116905483
10	91171168	91171169	T	C	35	GENIC	possibly homozygous	116905485
10	91171193	91171194	G	A	34	GENIC	possibly homozygous	116905487
10	91171341	91171342	G	C	25	GENIC	possibly homozygous	116905489
10	91171487	91171488	A	G	31	GENIC	possibly homozygous	116905491
10	91171761	91171762	A	G	24	GENIC	possibly homozygous	116905493
10	91171884	91171885	C	T	21	GENIC	possibly homozygous	116905495
10	91172051	91172052	T	C	13	GENIC	possibly homozygous	116905497
10	91172065	91172066	C	T	16	GENIC	possibly homozygous	116905499
10	91181269	91181270	A	G	16	GENIC	homozygous	116821815
10	91183970	91183971	G	C	27	GENIC	possibly homozygous	116905501
10	91184569	91184570	T	C	28	GENIC	homozygous	116821821
10	91185340	91185341	A	G	4	GENIC	homozygous	117258880
10	91177732	91177733	A	C	25	GENIC	possibly homozygous	116677052
10	91173670	91173671	T	C	22	GENIC	homozygous	116677050