chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	85684955	85684956	T	G	20	GENIC	homozygous	116815484
10	85685439	85685440	A	G	22	GENIC	homozygous	116666279
10	85685811	85685812	T	C	25	GENIC	homozygous	116666281
10	85686161	85686162	A	G	26	GENIC	homozygous	116666287
10	85686829	85686830	C	T	34	GENIC	homozygous	116815486
10	85687564	85687565	C	G	46	GENIC	homozygous	116815488
10	85687845	85687846	G	A	50	GENIC	homozygous	117018949
10	85689557	85689558	A	G	31	GENIC	homozygous	116666291
10	85689974	85689975	G	A	16	GENIC	homozygous	116815490
10	85689987	85689988	G	A	20	GENIC	possibly homozygous	116666293
10	85690306	85690307	G	A	28	GENIC	homozygous	116815492
10	85690979	85690980	T	C	29	GENIC	heterozygous	117018952
10	85692742	85692743	C	T	35	GENIC	possibly homozygous	116815494
10	85693963	85693964	T	C	29	GENIC	homozygous	116815496
10	85696131	85696132	C	G	61	GENIC	heterozygous	118004928
10	85696139	85696140	C	G	59	GENIC	heterozygous	118004929
10	85697768	85697769	T	C	34	GENIC	homozygous	116666309
10	85698433	85698434	G	A	41	GENIC	homozygous	116815498
10	85699346	85699347	C	T	53	GENIC	homozygous	116815500
10	85699639	85699640	G	A	29	GENIC	homozygous	118004930
10	85699647	85699648	A	G	29	GENIC	possibly homozygous	118004931
10	85699766	85699767	T	C	31	GENIC	homozygous	118004932
10	85699804	85699805	A	T	35	GENIC	homozygous	117018954
10	85704703	85704704	G	T	27	GENIC	possibly homozygous	116815502
10	85693669	85693670	G	A	30	GENIC	heterozygous	117105079
10	85695575	85695576	A	G	30	GENIC	homozygous	116982259
10	85696140	85696141	T	G	54	GENIC	heterozygous	118106376
10	85696168	85696169	G	A	80	GENIC	heterozygous	118106378
10	85696175	85696176	C	T	87	GENIC	heterozygous	118106380
10	85702549	85702550	T	C	32	GENIC	homozygous	116666315
10	85702839	85702840	A	G	32	GENIC	homozygous	116666317
10	85706674	85706675	C	A	40	GENIC	homozygous	116666329
10	85707478	85707479	G	A	50	GENIC	homozygous	116815504