Tag | Content |
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EnhancerAtlas ID | HS187-10513 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr17:42294070-42295530 |
Target genes | Number: 12 | Name | Ensembl ID |
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SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr17:42294446-42294464 | GGAGGGAAGCAGGGAAGC | + | 6.04 | EWSR1-FLI1 | MA0149.1 | chr17:42294442-42294460 | AGAAGGAGGGAAGCAGGG | + | 6.17 |
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| Number of super-enhancer constituents: 31 | ID | Coordinate | Tissue/cell |
SE_01039 | chr17:42294991-42295955 | Adrenal_Gland | SE_07447 | chr17:42294693-42301894 | Brain_Hippocampus_Middle_150 | SE_15256 | chr17:42291059-42300054 | CD4_Memory_Primary_7pool | SE_15781 | chr17:42292728-42294747 | CD4_Memory_Primary_8pool | SE_15781 | chr17:42295145-42299891 | CD4_Memory_Primary_8pool | SE_19807 | chr17:42292724-42300093 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_25059 | chr17:42295343-42300184 | Colon_Crypt_3 | SE_26749 | chr17:42294558-42301391 | Esophagus | SE_30189 | chr17:42294985-42297017 | Fetal_Muscle | SE_31591 | chr17:42294975-42300703 | Gastric | SE_34401 | chr17:42294580-42300622 | HCT-116 | SE_41411 | chr17:42294831-42301568 | Left_Ventricle | SE_42551 | chr17:42294668-42301533 | Lung | SE_47618 | chr17:42295162-42295888 | Pancreas | SE_50724 | chr17:42291607-42301523 | Sigmoid_Colon | SE_53422 | chr17:42292615-42300803 | Spleen | SE_55199 | chr17:42292654-42295961 | Thymus | SE_56585 | chr17:42294854-42300447 | u87 | SE_57187 | chr17:42294791-42295964 | VACO_400 | SE_59183 | chr17:42275072-42300390 | Ly3 | SE_60602 | chr17:42275172-42299512 | DHL6 | SE_62101 | chr17:42275357-42299503 | Toledo | SE_62375 | chr17:42274931-42300620 | Tonsil | SE_63277 | chr17:42294773-42299422 | GLC16 | SE_63317 | chr17:42276126-42299646 | NCI-H82 | SE_65631 | chr17:42294761-42296309 | Pancreatic_islets | SE_66786 | chr17:42293669-42295865 | Jurkat | SE_67389 | chr17:42293005-42299885 | MM1S | SE_68246 | chr17:42263244-42300248 | TC32 | SE_68247 | chr17:42263244-42300248 | TC32 | SE_68248 | chr17:42263244-42300248 | TC32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | GTCTGGTAAA GAGTAACAGA GGCCATCATG CCTGGCTCAT GCTATCCCCC CGATCTGTTC 60 CCCAGTTCTT GAGTGCTCAA CTCTTCCTCC CTAGGGCATC CCAGCCCCTG GTTGCTTCCC 120 ATCTGAAGGC ACAGACAAGA TATGGCTCAG CCCTAAGGAA ACTGTGGCCA TATTGGATCA 180 GGGCAGGGAC TCCAGTCCAG ACCATGCTAT ACCTAGAAAG CCAGGCTCGA ACTCAAGTCT 240 GGCTTGCTTC AAGGCTATTA TCATTTATAC TGTGCCAAGC TGCAACGGGC AGCTATTTGC 300 TGTAAGGGGA AGAGGGGTGG AAATGAAGGT ACAGTGATTC AGGGCTTTGT GGGAAACGAG 360 GTAGCTTGTC AGAGAAGGAG GGAAGCAGGG AAGCAATATA TCTAAATGTG CTGCCAAGTT 420 CAAGTTCTGA GTGGATATTC TAAATGTGCA ACGACTGAGA ATGGGGTGTG GACAGTAAGG 480 AAAATCCATG CAGATGTCTC TCCTGCACAG CTGGAAACCA ATGTTAGAGA CACCCACCAC 540 CCCCTAGCCC CTTAAAGCAG ATCAAGGGAG AATTTCTGGC AAATAAGAAA AAGGAAACAG 600 AAGCAGAAGC AGGATACAGG GCAGCTCTGA GGCAAGGTAG GCAGGTGCAC AGAAACTCTC 660 AGGGCCCTGC TCCAGGGAGA ACCCCCAGAA TTACAAGCTG TCTTGTCAGC CCAACTACCC 720 AGGGAAGCAA GAACAGGTCT GGAACAGTTA TTTTTCAGCC ACTGAAATGC AGCCCCAGAG 780 AGCTCTAGGC CACTGTGGAT GGGCTGGGAG AATAGCCACC CAAGGCCAGA AGTCAAAAGG 840 GCTCTCCATT TTCATTTGCA TCTGGTAACC TGGGCCAGAG ATTCTGCAGA ATGGGCCACG 900 TGGACCCATA ATCCCCTCTC CCCTCAATGT CCCACAAGCA TGGCCAGCTG TCCAGCTTCA 960 TCCTACTCTC TATCCCCATC TAGACTGGAT CACTGCTGAA TGAGGCAGAG ATCTAGTTGA 1020 GTACATATAT CCCATGGCTT GGGGCCTAAA ACCACCAAAA CAGCCCTTTT CTCCACCTGC 1080 CTCTACAAAA GCCTCATGGT CTTCCTAAAA AGCCTGAGAA GCCTTCCCCA ACCCCTTCCT 1140 GACCCTTCCT CTACACTCAT CCTTCCTCCC ATTCCAGGAC ACTGGGCTGG GACACACTTC 1200 AGGCTGAATG GGAACCCCAG AAGGCAGGCC TCCTCTAACA CAGAGGGTGA GGGACAGGGA 1260 GAGAGGGGAG GTGAGCCACT CCAGGCCAAA TAATTTGGAT TCAGCCAAAC CCCAAGTGTG 1320 GGAGATGCTT GATTCATAAA TACTCAAGGC ACTTTCTCCC CCAGTTCAGT GTATGCAGAC 1380 TGAAAAAGCC CTTGAAGAAG GGAGTGAGCC CCGCAGCCAC GAGGGAAAGA GGGTTTAAGT 1440 TTCAGAGGGC CGGGGGTGGA 1460
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