#chr	start	end	strand	id	ref	alt	so_term	validate	minor_allele_freq	is_supvar	in_supvar
11	69331642	69331642	+	rs554219	C	G	SNV	1	0.114325	0	0
4	145488334	145488334	+	rs1542725	C	T	SNV	1	0.294307	0	0
16	209709	209709	+	SNP195	T	C	SNV	1	NA	0	0
17	69108655	69108655	+	rs1859961	A	G	SNV	1	0.00367309	0	0
10	123333997	123333997	+	rs7895676	C	T	SNV	1	0.376033	0	0
8	128413305	128413305	+	rs6983267	G	T	SNV	1	0.436639	0	0
10	123340432	123340432	+	rs35054928	C	-	deletion	1	0.485767	0	0
5	159894847	159894847	+	rs57095329	A	G	SNV	1	0.117539	0	0
1	109817590	109817590	+	rs12740374	G	T	SNV	1	0.18641	0	0
8	128531689	128531689	+	rs11986220	A	T	SNV	1	0.103765	0	0
10	123340311	123340311	+	rs2981578	C	T	SNV	1	0.37787	0	0
11	69379161	69379161	+	rs75915166	C	A	SNV	1	0.0284665	0	0
11	69234620	69234620	+	rs7948643	T	C	SNV	1	0.203857	0	0
17	69107816	69107816	+	rs8072254	A	G	SNV	1	0.353076	0	0
16	52599188	52599188	+	rs4784227	C	T	SNV	1	0.21809	0	0