| Tag | Content |
|---|
EnhancerAtlas ID | HS092-09854 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr11:75849660-75851750 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr11:75851104-75851122 | CCCTCCCTCCCTCCCTCC | - | 6.03 | | EWSR1-FLI1 | MA0149.1 | chr11:75851108-75851126 | CCCTCCCTCCCTCCCTCC | - | 6.03 | | EWSR1-FLI1 | MA0149.1 | chr11:75851134-75851152 | CCCTCCCTCCCTCCCTCC | - | 6.03 | | EWSR1-FLI1 | MA0149.1 | chr11:75851138-75851156 | CCCTCCCTCCCTCCCTCC | - | 6.03 | | ZNF263 | MA0528.1 | chr11:75851114-75851135 | CTCCCTCCCTCCCCCTCTCCC | - | 6.01 | | ZNF263 | MA0528.1 | chr11:75851142-75851163 | CCCTCCCTCCCTCCCTCTCTC | - | 6.11 | | ZNF263 | MA0528.1 | chr11:75851092-75851113 | CTCTCTCTCTCTCCCTCCCTC | - | 6.89 | | ZNF263 | MA0528.1 | chr11:75851180-75851201 | CTCTCTCTCTCTCCCTCCCTC | - | 6.89 | | ZNF263 | MA0528.1 | chr11:75851096-75851117 | CTCTCTCTCCCTCCCTCCCTC | - | 6.9 | | ZNF263 | MA0528.1 | chr11:75851130-75851151 | CTCCCCCTCCCTCCCTCCCTC | - | 7.23 | | ZNF263 | MA0528.1 | chr11:75851184-75851205 | CTCTCTCTCCCTCCCTCCTCT | - | 7.28 | | ZNF263 | MA0528.1 | chr11:75851100-75851121 | CTCTCCCTCCCTCCCTCCCTC | - | 7.43 | | ZNF263 | MA0528.1 | chr11:75851116-75851137 | CCCTCCCTCCCCCTCTCCCCC | - | 7.46 | | ZNF263 | MA0528.1 | chr11:75851122-75851143 | CTCCCCCTCTCCCCCTCCCTC | - | 7.4 | | ZNF263 | MA0528.1 | chr11:75851126-75851147 | CCCTCTCCCCCTCCCTCCCTC | - | 7.89 | | ZNF263 | MA0528.1 | chr11:75851104-75851125 | CCCTCCCTCCCTCCCTCCCTC | - | 7.97 | | ZNF263 | MA0528.1 | chr11:75851134-75851155 | CCCTCCCTCCCTCCCTCCCTC | - | 7.97 | | ZNF263 | MA0528.1 | chr11:75851138-75851159 | CCCTCCCTCCCTCCCTCCCTC | - | 7.97 | | ZNF263 | MA0528.1 | chr11:75851108-75851129 | CCCTCCCTCCCTCCCTCCCCC | - | 8.55 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_00205 | chr11:75851171-75852968 | Adipose_Nuclei |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I076140 | chr11 | 75851172 | 75852968 |
|
Enhancer Sequence | CCCCACAAAA CAGCAGAGCA GGATTTCTGG GGTGGGAGGA TGGCAGCGCA GGGTCACAGC 60
ATGAGGGGTT AAGCACCTGG CTCTAGCCAC ACACCAACAA GTCACCTTCA GTGTTCCGGG 120
CTGTTTCACC TGGTGCTTCC ACCCCTCGTG GGCTGGGCTG GCAAATGAAA GCTTGGCTTT 180
TCTGCACAGA ATAGACTGTC TGAGGTGGTG CTGATGTTCT CTTTTGGTTT GAGTACCTAG 240
TCAACCTGCA AGATGATTTA GAGAGGGACA CTGTTAGCAA ATGGTAGAGT AAAAACAAGG 300
CTTGCAAAAA TGTGTAGCTT ACCCAATTAT TGTGAATTTG GGCAACATAT TAACTATAAA 360
CCTAGATCGA GGCCAGCAGA TTTTGCCCTG TTTTGTTTTG TTTTTCTGGA GAACTAAACA 420
CTGTAATTTA CTAGTCTACT TGCCTAGTTC TATATGTACC CCAGTGACCA CGCCTAATTA 480
TGAAATCTCT CCTGGCACCA GTACTCACAG CCAGGCAGAG GAGTCTGACA GACCCAAGGA 540
TTAGAAGCCG TGTGGTTGCC CCTTCCCAAG AATAACCCTT GCTTGGGTGT CTGAGACTGC 600
AAGTATAATC CTGCATCAGA GGAGAGAGAG CAGGGAGCTG GGGCCAGGGC TTGTGGCTGT 660
AGACACAAGT GGAAGAAACC CCAGATCTCT TTTCTTTTCT AGGGCACTTC TTGCTATTGT 720
AATTTGAAAA TGTATTATTT GAATAATGAG GGATGTCTTT CTCCTGCAGG ACTGGTAGCT 780
CCTTGGAGGA AGGGCCTACT GGTCTTGCAT CTGTCTCCCT ACCCCAAGGC CAGGCACATA 840
TGGGAACTAT TTGTTGGGTG TGTGTAGTTT CAAGTTCTGC CTCTACCCCT GCCTAGTGGT 900
TGCCCTTCTG CAAGCCACTT AACCCTCTAT GCGTGTTTCC TCATCTGAAG CACGCAAGTC 960
AAATGATCTG TGTGTGCCTC CCTCTGCCTC TGGACCCAAT CTGTTCATAT GGTTGTATTG 1020
AAGCTAATTT CATCCACATA CAAGAATGTC TAGAGCTAGC ATAGTGTATA ACATAGCCAT 1080
CATTTCCAGG ATGTAGATAC TCTATTTCCA TTAACTGATT ATTATTTATT ATTTCAGACT 1140
TTACCCTGCT TTCTCTATAG GGTTTTTGTA AAGACTAAGT GAAATGATGT ATAGGAAATT 1200
ACTTCAGAAA TTATAAAGTT TGTATAACTG AACAATGATT GTTATTGCTG GCCCAAAGAT 1260
ACCCTCCTGA GAAGAAACTC AGACCCAAAA GACAGCATTG CAGACCAAGT ATTGTAAAAC 1320
ATATGTGTGG CTAGCCCCAT CAAAGAATGT ATTTCCCAAG TTAGTTTTTC ATTTTAAAAA 1380
AAAAAAAGGA ACCCCTCAAA AATTTTTTTT AATTTTTAAA ATATAACCTT GACTCTCTCT 1440
CTCTCCCTCC CTCCCTCCCT CCCTCCCCCT CTCCCCCTCC CTCCCTCCCT CCCTCCCTCT 1500
CTCTCTCTCT CTCTCTCTCT CTCTCTCTCT CTCCCTCCCT CCTCTGCCAG TCCTCTAATG 1560
CAAGGTGGTT AGCATTTGGG TGTTGGCAAG GTTGTTGGTC ATGAAATCCT TCTCACTGCC 1620
TCACTGAGCA TGGGCAAGTC ATGTAAATTC TCTGCCAGAT GAGGATGCCT GCTTTTCAAA 1680
GCTAAAATAA GAATTGAATT GAATACTAAA ACAAGAATGA GATTATGGAT AGCCCTTCAG 1740
AAATATGAAG TTAGTTATAT CCTTCACATG TTTTTCTTGC TAGATCCAGC CTGTCCAGTT 1800
ACTTCACCTC TTCCCCATAG GACAGGGTTT CTGTTCCCTG CCCTGCCTTG GGCCCTCTTC 1860
TCTAAATATA TTGCAGTGTG TCTGTATCCT GCTGGAAGGA AGCTCCCAAA GTTGGACCCA 1920
CATACCTCAT GTTGTTTTTT GCATTGAGAC ACTGCAATAA CTATTGTCTA AGATTGATTC 1980
TTATCTATTT TTATTAGCTC AGACCTAAGT ATGCTGTTCC CTGTCTCTGG ATCCAGAAGG 2040
CTTACACTGA GTTCTGAAGT CCAAAGTAAC TTCTTGTTTT TGTTTCTCTT 2090
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