[{"allele_string":"-/C","most_severe_consequence":"downstream_gene_variant","input":"9 22125503 22125502 -/C 1","end":22125502,"strand":1,"transcript_consequences":[{"distance":4406,"gene_symbol":"CDKN2B-AS1","gene_symbol_source":"HGNC","transcript_id":"ENST00000422420","biotype":"antisense","gene_id":"ENSG00000240498","consequence_terms":["downstream_gene_variant"],"strand":1,"hgnc_id":34341,"impact":"MODIFIER","variant_allele":"C"},{"strand":1,"gene_id":"ENSG00000240498","consequence_terms":["downstream_gene_variant"],"hgnc_id":34341,"impact":"MODIFIER","variant_allele":"C","gene_symbol":"CDKN2B-AS1","distance":4408,"gene_symbol_source":"HGNC","biotype":"antisense","transcript_id":"ENST00000428597"},{"impact":"MODIFIER","variant_allele":"C","gene_id":"ENSG00000240498","strand":1,"consequence_terms":["downstream_gene_variant"],"hgnc_id":34341,"biotype":"antisense","transcript_id":"ENST00000577551","gene_symbol":"CDKN2B-AS1","distance":4931,"gene_symbol_source":"HGNC"},{"hgnc_id":34341,"gene_id":"ENSG00000240498","consequence_terms":["downstream_gene_variant"],"strand":1,"variant_allele":"C","impact":"MODIFIER","gene_symbol_source":"HGNC","gene_symbol":"CDKN2B-AS1","distance":4857,"biotype":"antisense","transcript_id":"ENST00000580576"},{"hgnc_id":34341,"consequence_terms":["downstream_gene_variant"],"gene_id":"ENSG00000240498","strand":1,"variant_allele":"C","impact":"MODIFIER","gene_symbol_source":"HGNC","distance":4931,"gene_symbol":"CDKN2B-AS1","transcript_id":"ENST00000581051","biotype":"antisense"},{"strand":1,"consequence_terms":["downstream_gene_variant"],"gene_id":"ENSG00000240498","hgnc_id":34341,"impact":"MODIFIER","variant_allele":"C","distance":4931,"gene_symbol":"CDKN2B-AS1","gene_symbol_source":"HGNC","transcript_id":"ENST00000582072","biotype":"antisense"},{"gene_symbol_source":"HGNC","gene_symbol":"CDKN2B-AS1","distance":4931,"biotype":"antisense","transcript_id":"ENST00000584020","hgnc_id":34341,"consequence_terms":["downstream_gene_variant"],"gene_id":"ENSG00000240498","strand":1,"variant_allele":"C","impact":"MODIFIER"},{"gene_symbol_source":"HGNC","distance":4931,"gene_symbol":"CDKN2B-AS1","transcript_id":"ENST00000584637","biotype":"antisense","hgnc_id":34341,"gene_id":"ENSG00000240498","strand":1,"consequence_terms":["downstream_gene_variant"],"variant_allele":"C","impact":"MODIFIER"},{"hgnc_id":34341,"gene_id":"ENSG00000240498","strand":1,"consequence_terms":["downstream_gene_variant"],"variant_allele":"C","impact":"MODIFIER","gene_symbol_source":"HGNC","gene_symbol":"CDKN2B-AS1","distance":4931,"biotype":"antisense","transcript_id":"ENST00000584816"},{"impact":"MODIFIER","variant_allele":"C","strand":1,"consequence_terms":["downstream_gene_variant"],"gene_id":"ENSG00000240498","hgnc_id":34341,"biotype":"antisense","transcript_id":"ENST00000585267","gene_symbol":"CDKN2B-AS1","distance":4959,"gene_symbol_source":"HGNC"}],"id":"9_22125503_-/C","assembly_name":"GRCh37","start":22125503,"seq_region_name":"9"}]