Tag | Content |
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EnhancerAtlas ID | HS047-15674 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr18:9651420-9652550 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr18:9651706-9651726 | CCCCCACCCACCCACCTGCC | + | 6.56 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_27340 | chr18:9651319-9652029 | Esophagus |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH18I009651 | chr18 | 9651320 | 9652029 |
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Enhancer Sequence | GGACTAGAAA AGCAGGTCAG CTGAAATAAC TTAGTGTGGG TATTTTTACT AAAAATTGGT 60 CAAATAGAAT CCTTTTAGAG ACAAATACTG AAATATTTAC AGGTGAAGTG ATGTGCTGGG 120 AGTTGTTTCC CCAGGGGGCA AGTGGTTGAG GATACTGACA AAGGTGGCCA TCTCACTTCT 180 TTGGTATATG TCTGCAATTT TCAAAGTAAA GTTTTAAAAA TGATCAGATA GATAAAATCA 240 TTTATTCTAT CATCAAGCAA ATGTCAAGAT ATGTCCTTTG CTGTGACCCC CACCCACCCA 300 CCTGCCAAAC TAACCTCACT GGCATTCCTT AATCCCTCTG ATGCAGTCCT GCCTCTGTGC 360 CCTAGGAACG CTGTTGACTC AGCAGGAGGC ATCTTGGCTG ATGTAGAGGT TCCCTTACTT 420 TGAAGGTGTC CTTGTTGGGG TGCCCTTGTC TGCTGTCATT ATCCTCTTCT AGTTCCTGCC 480 CCTACCTTGA GCTTCAGGAC TCCTGTATGA CCTGGTTCTT TTTTTTTTTT TTTTTTTTTG 540 AGACAGAGTC TTGCTCTGTT GCCCAGGCTG GAGTGCAGTG GCATGATCTC GGCTCACTGC 600 AACCTCCATC TCCTAGGTTC AAGCAATTCT TCTGCCTCAG CCTCCCCAGT AGCTTGGACT 660 ACAGGTGCCC GCCACCACGC CTAGGTAATT TTTTGTATTT TTAGTAGAGA CAGGGTTTCA 720 CTGTGTTAGC CAGGATGGTC TCAATCTCCT GACCTCGTGA TCTGCCCATG TCAGCCTCCC 780 AAGGTGCTGG GATTACAGGC GTGAGCCACC GTGCCGGCCT GACCTCCTTC TTGACTCATA 840 GTCTTTATCC GACCTCCCAT ACCTGCTTGG CCAGATGCAT TGCAGAGGAC TTACTACCCA 900 TGTGCTTCTG GTCTTCTGAC TTCTCCCTTG AATACGGAAT CTGGCAATTA AGCAACTCCC 960 AGGTTCAACC CAATTTCATG CTTGGTGCAT AATTCCCACC CTCCCCTGAC AAGTCTCCAT 1020 GATTAACTGG AGCTCACAGT TCACAGTGAC TCTGAAGGAG AAAAAAAACA ATTGCGCATT 1080 TTCAACTCAC AAGAATAACG TGCATTTCAT TTCTTTGTAG TTTTATTCTG 1130
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