chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5968566	5968567	G	A	11	GENIC	homozygous	45391208
20	5968631	5968632	G	A	12	GENIC	homozygous	45391212
20	5968674	5968675	T	C	7	GENIC	homozygous	45391214
20	5968814	5968815	A	G	17	GENIC	homozygous	45391218
20	5969033	5969034	C	T	8	GENIC	homozygous	45391230
20	5969060	5969061	T	C	10	GENIC	homozygous	45391232
20	5969087	5969088	T	C	11	GENIC	homozygous	45391234
20	5969092	5969093	A	G	10	GENIC	homozygous	45391236
20	5969200	5969201	C	T	7	GENIC	homozygous	45391244
20	5969334	5969335	T	TTCC	8	GENIC	homozygous	45732901
20	5969061	5969062	G	T	10	GENIC	homozygous	45818618
20	5969437	5969438	A	G	8	GENIC	homozygous	45391256
20	5969468	5969469	C	T	8	GENIC	homozygous	45818619
20	5969469	5969470	T	G	8	GENIC	homozygous	45391258
20	5969560	5969561	G	C	11	GENIC	homozygous	45391262
20	5969728	5969729	G	T	12	GENIC	homozygous	45391264
20	5969739	5969740	C	T	13	GENIC	homozygous	45391266
20	5969841	5969842	C	T	10	GENIC	homozygous	45391268
20	5969930	5969931	A	ACG	12	GENIC	homozygous	45673133
20	5969960	5969961	T	C	11	GENIC	homozygous	45673134
20	5969969	5969970	T	-	9	GENIC	homozygous	45732903
20	5969970	5969971	G	C	7	GENIC	homozygous	45862230
20	5970015	5970025	CCTTTTCCCA	----------	8	GENIC	homozygous	45732904
20	5970048	5970049	A	T	9	GENIC	homozygous	45673135
20	5970133	5970134	C	A	17	GENIC	homozygous	45391270
20	5970138	5970139	G	A	16	GENIC	homozygous	45391272
20	5970304	5970305	C	T	11	GENIC	homozygous	45673136
20	5970319	5970320	C	T	10	GENIC	homozygous	45673137
20	5970731	5970732	T	G	7	GENIC	homozygous	45391276
20	5970734	5970735	C	T	7	GENIC	homozygous	45391279
20	5970792	5970793	G	A	7	GENIC	homozygous	45732906
20	5971020	5971021	G	A	10	GENIC	homozygous	45732908
20	5971169	5971170	T	G	9	GENIC	homozygous	45391286
20	5971341	5971342	A	G	7	GENIC	homozygous	45391294
20	5971403	5971404	G	T	17	GENIC	homozygous	45391296
20	5971629	5971630	A	G	13	GENIC	homozygous	45391298