chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	85113760	85113760		G	21	GENIC	homozygous	129179169
14	85116441	85116442	G	T	9	GENIC	heterozygous	134102971
14	85122407	85122411	CAAT		11	GENIC	homozygous	129179171
14	85122552	85122553	C		8	GENIC	homozygous	129179172
14	85122588	85122588		T	9	GENIC	homozygous	129179173
14	85122629	85122630	T		6	GENIC	homozygous	129179174
14	85122658	85122659	G		8	GENIC	homozygous	129179175
14	85122680	85122681	G		10	GENIC	homozygous	129179176
14	85122689	85122690	G		10	GENIC	homozygous	129179177
14	85122696	85122696		G	10	GENIC	homozygous	129179178
14	85122705	85122706	T		10	GENIC	homozygous	129179179
14	85122717	85122718	A		11	GENIC	homozygous	129179180
14	85122728	85122729	T		10	GENIC	homozygous	129179181
14	85122745	85122748	CCG		9	GENIC	homozygous	129179182
14	85122757	85122758	A		10	GENIC	homozygous	129179183
14	85122795	85122796	T		11	GENIC	homozygous	129179184
14	85122812	85122812		C	11	GENIC	homozygous	129179185
14	85122820	85122820		G	10	GENIC	homozygous	129179186
14	85122830	85122831	G		10	GENIC	homozygous	129179187
14	85122890	85122891	A		8	GENIC	homozygous	129179188
14	85122896	85122896		T	8	GENIC	homozygous	129179189
14	85122929	85122929		T	6	GENIC	homozygous	129179190
14	85122930	85122930		TCT	6	GENIC	homozygous	129179191
14	85122945	85122945		TG	3	GENIC	homozygous	129179192
14	85122954	85122954		T	3	GENIC	homozygous	129179193
14	85122960	85122960		G	3	GENIC	homozygous	129179194
14	85125447	85125450	TTT		17	GENIC	homozygous	129179208
14	85125603	85125604	T	G	14	GENIC	homozygous	118703954
14	85122595	85122596	C	G	9	GENIC	homozygous	113501796
14	85122854	85122855	T	G	8	GENIC	homozygous	113501798
14	85122862	85122863	G	A	9	GENIC	homozygous	113788907