ENAapplication/xmlftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR249/099/SRR24965199/SRR24965199.fastq.gzprimaryOK200GenomicsUniversity of Phayaohttps://www.ebi.ac.uk/ena/browser/view/PRJNA985399Polymorphism 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 individualsENAfalseCharacterization of genetic variation in promotors of HBG1 and HBG2 gene2023-06-222023-06-22PRJNA985399