{"database":"ENA","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Fastqsanger.gz":["ftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR249/099/SRR24965199/SRR24965199.fastq.gz"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":null,"additional":{"omics_type":["Genomics"],"center_name":["University of Phayao"],"full_dataset_link":["https://www.ebi.ac.uk/ena/browser/view/PRJNA985399"],"long_description":["Polymorphism occurring in the HBG2 gene on chromosome 11 is an inherent modifier in beta-thalassemia which is strongly associated with increased HbF expression in beta-thal diseases, sickle cell disease, and healthy individuals"],"repository":["ENA"],"additional_accession":[]},"is_claimable":false,"name":"","description":"Characterization of genetic variation in promotors of HBG1 and HBG2 gene","dates":{"last_updated":"2023-06-22","first_public":"2023-06-22"},"accession":"PRJNA985399","cross_references":{}}