[{"regulatory_feature_consequences":[{"regulatory_feature_id":"ENSR1_9DX4","variant_allele":"C","impact":"MODIFIER","consequence_terms":["regulatory_region_variant"],"biotype":"promoter"}],"id":"rs901011140","end":955277,"colocated_variants":[{"strand":1,"frequencies":{"C":{"gnomadg_remaining":0.0004826,"gnomadg":8.696e-05,"gnomadg_mid":0,"gnomadg_amr":6.626e-05,"gnomadg_nfe":0,"gnomadg_sas":0,"gnomadg_afr":0.0002677,"gnomadg_ami":0,"gnomadg_asj":0,"gnomadg_eas":0,"gnomadg_fin":0}},"id":"rs901011140","seq_region_name":"1","allele_string":"G/C","start":955277,"end":955277}],"seq_region_name":"1","most_severe_consequence":"upstream_gene_variant","input":"rs901011140","strand":1,"assembly_name":"GRCh37","allele_string":"G/C","start":955277,"transcript_consequences":[{"transcript_id":"ENST00000379370","variant_allele":"C","hgnc_id":329,"strand":1,"gene_symbol_source":"HGNC","gene_symbol":"AGRN","consequence_terms":["upstream_gene_variant"],"biotype":"protein_coding","gene_id":"ENSG00000188157","distance":226,"impact":"MODIFIER"}]}]