Tag | Content |
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EnhancerAtlas ID | HS092-38635 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr9:116942190-116944780 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESRRB | MA0141.3 | chr9:116944124-116944135 | TATGACCTTGA | - | 6.62 | Esrrg | MA0643.1 | chr9:116944125-116944135 | ATGACCTTGA | - | 6.02 | RORA | MA0071.1 | chr9:116944126-116944136 | TGACCTTGAT | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_02066 | chr9:116942167-116944464 | Aorta |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I114180 | chr9 | 116942477 | 116944847 |
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Enhancer Sequence | TCACTGCAGC CTCCACCTCC CAGGTTCAAG GGATTCTCCT GCCTCAGCCT CCCAAGTAGC 60 TGGGATTACA AGCACACGCC CCCGGGCCCA GCTATTTTTT CGTATTTTTA GTAGACATGG 120 GGTTTCACCA TGTTAGCCAG GCTGGTCTCA AACTGCTGAC CTCAAGTGAT CCACCTGCCT 180 CGGCCTCCCA AAGTGCTGGG ATTATGAGTG TGAGCCACTG CGCCTAGCCC AGAGCCTACC 240 ATCTTAAGCA TCTATTGTGC TTATTTTTCT GAGTATTCAC CTGAGCCCCT CCAGAGATAG 300 GCCTCGGTTA CCTCTCTCTC CTACGTGATG CCTGGCAGAG CACCCTGCGT GCTGGAGGTG 360 CTGGGCAAAT GATTGGTGAA GAGTTCTAAT GTAGGAGTCA AGAATATTTC TACCAAGAAG 420 TTGTGGAATC TTAGGCAAGT CCCTTCTGTC CTTCTAGGCT CAGTTTCCCC ATCTATAAAG 480 GCTGGGGTCA TGGTAAGGCA TTTCTAAGTT TCCACCTAGC TCTGGGTGAA TGACTCTCCT 540 GACACGCTTC TAGGCTCTTT GCCTGCACGC CACCCCAACT CTCCCTGCCC GCCGTCCCAC 600 CATCATCCTG TTTCTAGACT GGAAATTCCA TAGATTATAA AATTCCAAAG ATAATAGAAT 660 GCTGGATTAA ACAATCCCAG CTCCTCTCTG CACAGATGGG GGCTCTGGGG CTTAAGGAGG 720 GGCATTCTTA CCTGAGGTCG CCCAAAGCTC TCTGTCTTGC CCCTTCCTAC CTCCACATAT 780 TCCCCCAGCC CATGGAGGGA TGTTGGGGAA TCCCAGAGCC TCCCCCACCT GGCTTTCTAG 840 GCTGCAGCAT TTATAGAATT GGTCTGCTTG GCTTTCAGTC AACTATGTGC CTCGTTTCTC 900 TGCAATACTG GAGAGGGTTG GGGACGGGGG GGCAGGGAAA CAGGAAGCCC CCACCTTCAG 960 AAGCTGCAGA TGGGGGAGCT GAGTGCTCTG GCCCACCATC TGTGGGGCAG CTGGGGCACG 1020 ACTGGGGAGA GGCAGCCGCC CTTGACCTTG TGCAGCCTAC GCCTGGCTCT GGTGGAACTG 1080 GGTGTCAGGA ACCCCTCCTT GAACACTCCC TCCCAACCTC TGTCCAATTC CCACTGAGCT 1140 TGTGGTTAGA CCTGGTTAGA CCCCACAAGC CTGGGCTGGG GTGAACATCG GAGGGTGTTC 1200 CAGATTCCTT AGAGACTGCT GGGTCCCAGT CACTTACAGA ACAGAGGGAG AGACCGAGGC 1260 TGGGGATTAT GAGGTGGGGC TCAGAATTGG GACTCAGTCT CGATGCTTCC AGGTTCTGTC 1320 GCGTGCCAGG AGACAGTGTT TGGTGGACTG CAGGGGAGGG CAGGAGGGCT GATTATTTTG 1380 GAAGGAGGGT CACAAGAGGC ACTGAGAAAC TCCCCAGGCT CAGTGTGCTC TGGACACTGT 1440 TCCTTGCCGG TGCATTCGGA GAAGGGGAGG GTCCCAGTTC AGGCATCAAG GAAGAGAGGA 1500 AGAGGGAGGT GCCTTGGTTG GAATGTGACA GGCTGCAGCT GGGAAGCTGG CCTCAGAGAG 1560 GGAAGAAGAA AGCAGTTCAC ACACAGTTAG CCCGATGAAT CAAGAGGGAC GGGGAAGAGG 1620 GCAGTGTGCC TAGAGGCTGG TGGGGTTGGG AGGACCACTG GACCCTTGAG GGTGCCTCTC 1680 CTCACCTCCT ATGCCCCAGA TTATTCCTGC TAGACAAAAA CCCTCAAGTA TTCCCCGGCT 1740 CTTAGGGCTC TATTTATATT ACTGTGCTGG AAGACTCTAG GCCAGGGCCC TTGCTGGAGA 1800 AAGTGGACAT AACAGGACCC AGCTGTTATC GGGGAACTTG GATATGGCCT GGGAAAATCC 1860 AGCGCCATGA ATAAACTCTG GACTTGAAGC CACCAGGCCC TGGACCCTGA TCTCACTTGG 1920 CCACAAATCT GCTGTATGAC CTTGATCAAG CCTCCTGGAC TCTCTGGGTC CAGTGTTCCC 1980 AGGTGCTCTG TGGTCTCTGG AAGACCTTGA AAGCTTGGAG CTTGCAGGTG TCTAAGGGTC 2040 TGATCACGTG TTGTAGCCAC AGGAGAGGTG CACCTTTGTT CACAAGAGGT CAAATACATC 2100 CTTCTTGAGC TCTCAACTCC AAAGACTCAT ACAAAAGTCC AGTTGGGGCC AGCTGCCGTG 2160 GCTCACGCCT GTAATCCCAG CACTTCAGAA GGCCAAGGCA GGAGGATTGC TTCAGGCCAG 2220 GAATTCGAGA CCAGCCTGGG CAGCATAGCA AGACTCCATC TCTATAAAAT AATAATAATA 2280 AAATAATAAA AATAATAAAA TAAAAATAAT AATAAAATAA TAAAAATTAG TGGCCCATGC 2340 TTGGAGTCCC AGCTACTCAG GAGGCTAAGG TGGGAGGATC TCTTGAGCCG AGGAGTTTGA 2400 GGCTGCAGTG AGCCATGATC ATACCACTAC AGTCTAGCCC AGGCGACAGA GCAAGACCCT 2460 GCCTCTAAAA AAAAAAGTCC ACTTGAGACT GGAGGAGCCC TAGAGGGTTC CCCGGAGGAG 2520 ATGGCACTTT GAGCCAGGCC TGAAGGATGG ATCAGGTTTC AAGCAGAGGA GATGGATGAG 2580 AAAAGATGCT 2590
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