Tag | Content |
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EnhancerAtlas ID | HS047-02650 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr1:183588350-183589700 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr1:183589314-183589327 | TTCTGGAATGTTC | + | 6.59 | TBX21 | MA0690.1 | chr1:183589440-183589450 | TTCACACCTT | - | 6.02 | TBX2 | MA0688.1 | chr1:183589439-183589450 | TTTCACACCTT | - | 6.62 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_65086 | chr1:183588357-183590217 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 183588950 | 183589185 | chr1 | 183589393 | 183589695 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I183619 | chr1 | 183588358 | 183590217 |
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Enhancer Sequence | TTCCATTACC TTCCCAAATC CTATAAAACG GCCCCACCCT TATTTCCCTT CACTGACTCT 60 CTTTTTGGAC TCAGCCCACC TGCACCCAGG TGAAATAAAC AGCTTTATTG CTCACACAAA 120 GCCTGTTTGG TGGTCTCTTC ACATGGACGC GCATGAAACC TGGGACTCTG GAAGTGGAAC 180 TGAGAAAGAA AAGTCAGTTT TGGTCTGGGT GCCTGAACAT CATGATGGAA AACTTAGGGG 240 GTTTCTGGTG GAGTGTTTTG TCATGTTACT GGTAAAGCAG AGGAGACTGA TTATTGGTGA 300 TAAAAGCAAG AATGGAGCAG ACCTGCAGAG AAATGTAAGC ATGAGTTTTC AGTGGCTGGT 360 ATATAAAAGT TAAGCAGAGC TTTATGCAGT ATTAAACAAT ATTATTACAG CTCCCAGAAG 420 CCCGGTTTAT ACTGATTTCA TATGAACGGC ACCCCTTACA GCACAACTGT GTGGCATGAA 480 TGGTGTCCCC TGGACTTGTG CTATGAGGCA GTCCTACTTT TAGTTGGGGA TGGGGCTGTA 540 GATAAAGGCC AGGGCCAAAT AATGCAGATA TTGTATATCA TTTAGAGCAG GAATAAAATA 600 TGTGTTGTGA TTCTACATGT CTAAAACCCA TGGCAGACAT CACTAATTCT CATGGTCCAC 660 CTACCTGTTG AACTCCAACA TGTCCTACTC AATACAGCAC CCCAGAGAGT CACTATCAAT 720 CAGCATATAC TTTGTCTATG TACTTCCTGG CCTGACAACA GCTATAACAT GAAACTCATA 780 AGTAGCTGTA TCTCAGCAGC AGATGGTTTC CCTCTCGTTA GAATAAACAC TGGGTATTAT 840 ATCAAAGTTA AGGAAATCTT TTGCTTTTGA TCTGAGGACC CAGAAAATTT GGAACCAGTC 900 TTCAAACTTA GTGGTAACAT GGTATCACTT AATTAACTTG ATTTAATACT AATAATGAAC 960 AGGATTCTGG AATGTTCACT AATTGTGTGA ATTCTGAAAT CGTGTTGTTT CCTCGGCTTG 1020 GTATTCCCTT CCTGTTTTCT ATTTGCCAAA CTCTTAGATA GCCTTCAAGG CCCATTGAAA 1080 TGCTCCCATT TTCACACCTT TTCCTTGACA TTCTCTCTTG GAGAAGTAAT TGCTCCCCAT 1140 CTGTTATTGT ACATGAATTT ACTCTCTTCT CTATTATAGC TTGTTTACTA TTGAATTTTA 1200 TTCATTGCTT GTGTATCTTA CCTAGAATCT AGATCCCACA GGATAAGGAT TGTATTTTAA 1260 ATATTTTAAG CAGCCCTTAG CATGTAAATA CTTGCCTGAA TGACAGTGAA ACTGTGCTTT 1320 CACGTGCGAA ATACTTTGGG TAGTTTGTCT 1350
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