chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	88997027	88997028	G	A	20	GENIC	homozygous	116950378
10	88997095	88997096	A	G	20	GENIC	homozygous	116950380
10	88997136	88997137	T	C	17	GENIC	homozygous	116950382
10	88997143	88997144	C	T	18	GENIC	homozygous	116950384
10	88997227	88997228	C	A	16	GENIC	homozygous	116950386
10	88998444	88998445	T	C	26	GENIC	homozygous	116950388
10	88998563	88998564	A	C	37	GENIC	homozygous	116950390
10	88998694	88998695	T	C	34	GENIC	homozygous	116950392
10	88999469	88999470	G	A	24	GENIC	homozygous	116950396
10	88999595	88999596	G	A	31	GENIC	possibly homozygous	117413092
10	88999757	88999758	G	A	35	GENIC	homozygous	116950398
10	89000201	89000202	G	T	19	GENIC	homozygous	116950400
10	89000354	89000355	G	A	13	GENIC	homozygous	116950402
10	89000380	89000381	C	T	6	GENIC	homozygous	116982497
10	89000504	89000505	G	A	20	GENIC	homozygous	116674932
10	89000750	89000751	T	C	32	GENIC	homozygous	116950404
10	89000807	89000808	T	C	30	GENIC	homozygous	116950406
10	89000945	89000946	C	T	34	GENIC	homozygous	116950408
10	89000998	89000999	C	T	32	GENIC	homozygous	116950410