Tag | Content |
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EnhancerAtlas ID | HS187-14981 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr20:1633460-1634700 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ELK1 | MA0028.2 | chr20:1633822-1633832 | ACCGGAAGTG | + | 6.02 | ERG | MA0474.2 | chr20:1633822-1633832 | ACCGGAAGTG | + | 6.02 | ETS1 | MA0098.3 | chr20:1633822-1633832 | ACCGGAAGTG | + | 6.02 | FEV | MA0156.2 | chr20:1633822-1633832 | ACCGGAAGTG | + | 6.02 | FLI1 | MA0475.2 | chr20:1633822-1633832 | ACCGGAAGTG | + | 6.02 | GATA2 | MA0036.3 | chr20:1633939-1633950 | TTCTTATCTGT | + | 6.14 | Gata1 | MA0035.3 | chr20:1633939-1633950 | TTCTTATCTGT | + | 6.62 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_17655 | chr20:1631554-1648922 | CD4p_CD25-_CD45RAp_Naive | SE_18473 | chr20:1630935-1648926 | CD4p_CD25-_Il17-_PMAstim_Th | SE_23025 | chr20:1631128-1643815 | CD8_primiary |
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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 | CAGTGGATGT AAGCAACAAA AGGGCAATTA CTTTTTCTCT TTTATTCTAC CAAAGTACCC 60 CATGTTTTTA TGTCAGATCC TGGCACATAG TAGGTATCCA ATAGATATGT GTGTAATGTT 120 TGAATTGCTC AGTGGGACAT TTCCCTCGAA GACTGAAATC TTCTATTTTA GGTGGTTTGC 180 TCCTGTGGAA TTTGACAGAA AATGAGTTTC CCATGTAGAG GACTTAGTGA AAAAAAATCA 240 GTTTGCAAAC ATACAGAAAG TAGAAGAGCC CAGAGAAGAA AACCACAATC TCCCTTCACA 300 CCACATTGCC CACTCCACAC CCAAGAGCAG CAGCTGCAGA AATCTCATGG AATAGAATCA 360 AGACCGGAAG TGTTTGAGTA ATGGTGAAAC CTGTGACCTC TAGAGTCAGA GTGCCTGAGT 420 TCAAATCGTA GCTCTACCAG TTACCAATGA GTGAGCCTGG AGCACTTTGT GCTTCTGTTT 480 TCTTATCTGT TAGGAAAGGT GACAAGAATA TCTACCTTGT ATATAATGAT CACATGAAGT 540 AAAAGAGGTA AGGCATTTTC AACAGTGTCT GCCACATGGT GAACGTTCAA AAATTGTAAA 600 GTTATTGCTC AGTAGATTTC TGAGGCTTGG AGGCTTCAGT GGACATTAGA TGACAAGGAT 660 AAGGATAAGG GTATGGATAT GGATATAAAT ATAACTATAG TTATAGGTAA TATAGGCAGA 720 CCTGTGTCAC CTGTATCCCC ACATTTTTTT CCTCATTTCT ACCTTCATGG AAGAGGGAAT 780 TTCAGGATAA AAATGCACAG AAATTCTGCT TTGAGGGAAA ATGCATTTTA CCAAGAGAGA 840 AGTTTGCTTA TCTGTTGCTT CTATTAACAG ATTGGAGGAC TTTCAGTGGT AAGATTAGAG 900 AAGTAGGAAG GAGGGAGAGT GGCTGGGCAA TAGGGAAAAC CACACATCTC TTCAATGTGC 960 ATTTCATATA GACTGAAAAA ATGAGTTGAA GTTTACAGTA AAGAAAGTCT TTAAAATTCT 1020 GTGTGTGTTT CAGCATGGTC ACATGAGATT TATCTCAGGA ATGCAAGGAT GGTATAACAT 1080 TCATAAATCT CCAAATGTGA TATGCTACAT CAAGGCAATC TTGAGCAAAA AGAACAAAGA 1140 TGGGGCCGGG CATGGTGGCT CATGCCTGTA ATCCCAGCAC TTTGGGAGGC CGAAGCGAGC 1200 AGATCACGAG GTTAGGCAAT CGAGACCGTC TTGGCCAACA 1240
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