chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	47525894	47525895	T	C	19	GENIC	homozygous	116773917
10	47526532	47526533	C	G	11	GENIC	homozygous	116878684
10	47528579	47528580	G	A	17	GENIC	homozygous	116878686
10	47530417	47530418	T	C	29	GENIC	homozygous	116773921
10	47530945	47530946	T	G	5	GENIC	homozygous	117103809
10	47533157	47533158	A	G	18	GENIC	homozygous	116773923
10	47533575	47533576	G	C	21	GENIC	homozygous	116773925
10	47535051	47535052	T	G	8	GENIC	heterozygous	116773929
10	47535896	47535897	T	C	8	GENIC	homozygous	116773931
10	47536400	47536401	C	T	8	GENIC	homozygous	116773933
10	47536501	47536502	A	T	12	GENIC	homozygous	126419634
10	47536903	47536904	G	T	4	GENIC	homozygous	116773935
10	47536924	47536925	A	G	4	GENIC	homozygous	116773937
10	47536953	47536954	G	A	15	GENIC	homozygous	116773939
10	47536954	47536955	T	C	15	GENIC	homozygous	116773941
10	47537227	47537228	C	T	14	GENIC	homozygous	116773943
10	47537304	47537305	G	A	17	GENIC	homozygous	116878688
10	47537485	47537486	C	A	27	GENIC	homozygous	116773945
10	47538988	47538989	T	C	20	GENIC	homozygous	116878690
10	47539003	47539004	C	T	19	GENIC	homozygous	116773947
10	47539382	47539383	G	A	30	GENIC	homozygous	116773949
10	47539902	47539903	C	A	15	GENIC	homozygous	116773951
10	47540370	47540371	A	T	19	GENIC	homozygous	116773953
10	47540949	47540950	C	T	21	GENIC	homozygous	116773955
10	47542392	47542393	A	G	19	GENIC	homozygous	116773963
10	47542519	47542520	A	C	19	GENIC	homozygous	116773965
10	47543290	47543291	G	A	30	GENIC	homozygous	116773967
10	47543361	47543362	A	G	12	GENIC	homozygous	116878692
10	47544113	47544114	C	T	21	GENIC	homozygous	116773971
10	47545453	47545454	G	C	20	GENIC	homozygous	116773975
10	47546372	47546373	T	C	8	GENIC	homozygous	116773977
10	47546384	47546385	C	T	7	GENIC	homozygous	116878698