Tag | Content |
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EnhancerAtlas ID | HS092-24386 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr2:97189370-97191050 |
Target genes | Number: 10 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BCL6B | MA0731.1 | chr2:97189419-97189436 | GGGTTTCCTAGAATGCA | - | 6.18 | ETV6 | MA0645.1 | chr2:97190855-97190865 | AGCGGAAGTG | + | 6.02 | EWSR1-FLI1 | MA0149.1 | chr2:97189390-97189408 | GGAAGGAAGGAAGGAAGG | + | 10.83 | EWSR1-FLI1 | MA0149.1 | chr2:97189370-97189388 | GGCAGGCAGGCAGGCAGG | + | 6.1 | EWSR1-FLI1 | MA0149.1 | chr2:97189374-97189392 | GGCAGGCAGGCAGGCAGG | + | 6.1 | EWSR1-FLI1 | MA0149.1 | chr2:97189398-97189416 | GGAAGGAAGGGAAGGAAG | + | 6.1 | EWSR1-FLI1 | MA0149.1 | chr2:97189403-97189421 | GAAGGGAAGGAAGAAAGG | + | 6.85 | EWSR1-FLI1 | MA0149.1 | chr2:97189378-97189396 | GGCAGGCAGGCAGGAAGG | + | 6.92 | EWSR1-FLI1 | MA0149.1 | chr2:97189382-97189400 | GGCAGGCAGGAAGGAAGG | + | 7.74 | EWSR1-FLI1 | MA0149.1 | chr2:97189394-97189412 | GGAAGGAAGGAAGGGAAG | + | 8.57 | EWSR1-FLI1 | MA0149.1 | chr2:97189386-97189404 | GGCAGGAAGGAAGGAAGG | + | 9.17 | Gata1 | MA0035.3 | chr2:97190085-97190096 | ACAGATAAGGA | - | 6.14 | KLF5 | MA0599.1 | chr2:97190637-97190647 | GCCCCGCCCC | + | 6.02 | SPIB | MA0081.2 | chr2:97190853-97190865 | GAAGCGGAAGTG | + | 6.44 | TFAP2C | MA0524.2 | chr2:97190542-97190554 | TGCCCGAGGGCA | - | 6.27 | TFAP2C | MA0524.2 | chr2:97190542-97190554 | TGCCCGAGGGCA | + | 6.52 | ZNF263 | MA0528.1 | chr2:97189396-97189417 | AAGGAAGGAAGGGAAGGAAGA | + | 6.05 | ZNF263 | MA0528.1 | chr2:97189395-97189416 | GAAGGAAGGAAGGGAAGGAAG | + | 6.24 | ZNF263 | MA0528.1 | chr2:97189391-97189412 | GAAGGAAGGAAGGAAGGGAAG | + | 6.31 | ZNF263 | MA0528.1 | chr2:97189399-97189420 | GAAGGAAGGGAAGGAAGAAAG | + | 6.56 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_43681 | chr2:97190155-97206675 | MM1S | SE_67180 | chr2:97190155-97206675 | MM1S |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 97190381 | 97190605 | chr2 | 97189513 | 97189979 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I096523 | chr2 | 97189411 | 97191322 |
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Enhancer Sequence | GGCAGGCAGG CAGGCAGGCA GGAAGGAAGG AAGGAAGGGA AGGAAGAAAG GGTTTCCTAG 60 AATGCACCAG GCCAAGACTA AGACCCAGAC CCCTCCCCAG CTATCCCAAT CTCCCTGTAG 120 TTGCTGGGGA TCCAGAGCCT GTCCTGCTCT CCCCCAGCCC AGGGTGCCCT TCCTGCCTTC 180 TCAGTGGCCG GGGTGCCCCT TTCCCTGTCT TTTTCCTGGC GTGCCCTCTG GCAAGGGAGT 240 GGGTCCTGAG CTGTGTGCAG GGTGCATGCG TGACACAGAG TGGGGTGGAA CAGAATCCCA 300 GGAAGGCTGA GCCCAGGCCC TGCCCTTCAT CCCCTGGCCC TTTCCCAGAG GAGGCACAAC 360 AAACTCAAAG AGAACGTATG GGCTCCAGAC CAAAGGTCCT TGGTTCATTG CATGCAGCTC 420 CCACGGCTGC AGCGGCTTTT ATGAGAAAGC AGCAAATCAT AAGAAAACTA TCTCCTTGGG 480 AGGACTTAAT TGGGACAGAA ACTGCAGATG GATGCCAGAT GTGCAACGGC ATCCAAACCC 540 GAGTCCCAAA TCCCCACAAA GATCCTCAGT CGACTCTCCC GATCCTTTGA CCAGGTAATA 600 AGAGTCCTAA TAGCAGTAGC AATGGCTCCA TTTCTAAAGC ACACACGGTA TGCTATGCAC 660 TGCTTTTATT TCTAGTTCCT TTCATTACCT AGAGAGGCAT TGCTCTGCAC ATTTTACAGA 720 TAAGGAAACT GAGGTTACTG AGGTTAGGTA ACTCAACCAA GGTCACATAT TTAGAAAGTG 780 GTGGAACTTT TCAAAATACT AAGTTGGGGA AATGCTCATC ATTTGTAGAA AAATTTTCAA 840 TAAGGCATAA GAACACAGGT TTCCAGTTAA CCCTCAGTTA CCCAGAAAAG TAAATTCCCC 900 AGAACGTCCT GCACATCGTG TATGCCTGTG TATGTGCATG CACTTGAATA TTCTGATTAG 960 CAGAGCTCGT GATAAACAGG CCAGACTACA GGGGAAAAAA ATGTGCAGAA ACCAGCAACC 1020 ATATTCTCCG AATTCATCGC ATGCTTGGAG ATCCCCAGGT AAAAAGTTAG CAAAACATAC 1080 CTTGTTCAAA ACAACTGGCC AAGGACGGGA TGTGAAGCAG CCACTGCTGC TAGGGGCACA 1140 GCATCCATTG GAGTTCCCTC CCCACCCCTA ACTGCCCGAG GGCAGCAGAT CCAGGGTTGC 1200 CCGGCCACCT CCCTCTCCTG ACTGCAGTGT GGGAAGAAAC GCAGGACGCT GGCAGGCACC 1260 AGACCGTGCC CCGCCCCTGA TCCACAGTGT GGCTTTGAGC ACACCACTTT CCCTCTCTGG 1320 GCCTTGGTTT TCCCATCTGT AAAATCAGGG CACAGTGAAC TGTAAAGGGC TCGGAGGGAA 1380 ATTTCATGGA CTGGTTGATG ATCCCAGGCT GCCGCCCTTT AGGAGAGGTC CTCCCTCCAG 1440 AGGGCTCTTG GACCTTGGGG ATCCCAGGTG GGAGCCTTCA TGGGAAGCGG AAGTGAGCCC 1500 TGAGACCTCT GCAGGCTTCT CTCCTACCTC TGAAAGACTG AGCAGGCAGC CTGGTGTCTC 1560 AGACACTCCT CATTTCCCTA CTTCCCTTCA ACAGGGTTAG AGTTCCTACG AAAGCTTTGC 1620 TGCCATGCAA GAAGGCAGAA TGCTCTCCCA CATGGAGACG CACCCAGACA GTCCACGGGA 1680
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