Fig. 2From: Identifying genetic variants and pathways associated with extreme levels of fetal hemoglobin in sickle cell disease in TanzaniaCharacterization of SCD gene function and exome map from the targeted next generation sequencing: This included the exon and full regions for validated and novel fetal hemoglobin-associated loci, including B-cell lymphoma/leukemia 11A (BCL11A), proto-oncogene, transcription factor (MYB), Homeobox A9 (HOXA9), Hemoglobin subunit beta (HBB), hemoglobin subunit gamma 1 (HBG1), hemoglobin subunit gamma 2 (HBG2), chromodomain helicase DNA binding protein 4 (CHD4), Kruppel like factor 1 (KLF1), methyl-CpG binding domain protein 3 (MBD3), zinc finger and BTB domain containing 7A (ZBTB7A), Peptidoglycan recognition protein 1 (PGLYRP1) on chromosomes 2, 6, 7, 11, 12 and 19, respectively. a gene functions from patients with high HbF levels and b gene functions from patients with low HbF levelsBack to article page