Tag | Content |
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EnhancerAtlas ID | HS016-00532 |
Organism | Homo sapiens |
Tissue/cell | CD14+ |
Coordinate | chr21:34754560-34756890 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr21:34754590-34754608 | GGAAGGAAGGAAGGAAGG | + | 10.83 | EWSR1-FLI1 | MA0149.1 | chr21:34754594-34754612 | GGAAGGAAGGAAGGAAGG | + | 10.83 | EWSR1-FLI1 | MA0149.1 | chr21:34754670-34754688 | AGAAGGGAAGAAGGAAAG | + | 6.03 | EWSR1-FLI1 | MA0149.1 | chr21:34754578-34754596 | GAAAGGGAGGGAGGAAGG | + | 7.45 | EWSR1-FLI1 | MA0149.1 | chr21:34754582-34754600 | GGGAGGGAGGAAGGAAGG | + | 8.32 | EWSR1-FLI1 | MA0149.1 | chr21:34754598-34754616 | GGAAGGAAGGAAGGAAAA | + | 9.07 | EWSR1-FLI1 | MA0149.1 | chr21:34754586-34754604 | GGGAGGAAGGAAGGAAGG | + | 9.47 | Foxd3 | MA0041.1 | chr21:34756589-34756601 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr21:34756593-34756605 | GTTTGTTTGTTT | + | 6.32 | Klf1 | MA0493.1 | chr21:34756066-34756077 | AGCCACACCCT | + | 6.02 | USF1 | MA0093.2 | chr21:34755676-34755687 | GCCACGTGACC | + | 6.62 | USF2 | MA0526.2 | chr21:34755674-34755690 | GCGCCACGTGACCCAG | - | 6.69 | ZNF263 | MA0528.1 | chr21:34754580-34754601 | AAGGGAGGGAGGAAGGAAGGA | + | 6.09 | ZNF263 | MA0528.1 | chr21:34754575-34754596 | GAAGAAAGGGAGGGAGGAAGG | + | 6.23 | ZNF263 | MA0528.1 | chr21:34754595-34754616 | GAAGGAAGGAAGGAAGGAAAA | + | 6.56 | ZNF263 | MA0528.1 | chr21:34754591-34754612 | GAAGGAAGGAAGGAAGGAAGG | + | 6.94 | ZNF263 | MA0528.1 | chr21:34754584-34754605 | GAGGGAGGAAGGAAGGAAGGA | + | 7.08 | ZNF263 | MA0528.1 | chr21:34754587-34754608 | GGAGGAAGGAAGGAAGGAAGG | + | 7.42 |
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| Number of super-enhancer constituents: 12 | ID | Coordinate | Tissue/cell |
SE_00219 | chr21:34750982-34756583 | Adipose_Nuclei | SE_09780 | chr21:34750609-34758167 | CD14 | SE_10653 | chr21:34751101-34757835 | CD19_Primary | SE_10924 | chr21:34750502-34759616 | CD20 | SE_27036 | chr21:34754548-34756615 | Esophagus | SE_36753 | chr21:34754454-34756616 | HMEC | SE_53413 | chr21:34751185-34757173 | Spleen | SE_58466 | chr21:34731200-34786233 | Ly1 | SE_60169 | chr21:34732700-34761220 | Ly4 | SE_60632 | chr21:34732666-34757447 | DHL6 | SE_61512 | chr21:34731229-34778660 | Toledo | SE_64665 | chr21:34754499-34756570 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr21 | 34754708 | 34755048 | chr21 | 34755296 | 34756154 |
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| Number: 1 | ID | Chromosome | Start | End |
GH21I033378 | chr21 | 34751108 | 34757769 |
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Enhancer Sequence | AAGAAAGAAA GAAAAGAAGA AAGGGAGGGA GGAAGGAAGG AAGGAAGGAA GGAAAAAGAA 60 AAGTAAAGAA CAGAAAAAGA AGAAAGGAAA AGAAAAGAAA GGAAAAGAAA AGAAGGGAAG 120 AAGGAAAGAG CAGAGAGGCC CAGTCGCTCT TCTCAGAGTC TCCGTGGCAT CTCGGTAGAT 180 TTGCTGATCC CTTTACATAA CCCAAGTTGA GGCATGCCCT AATTTCACCC ACAAATGCTA 240 CTAAGCCCAG GCCCTTATCC AGCCAAAACC ATCCTGCCAA GCTCCCACCA CCACCATCAG 300 CATCATTTTC AGGTTGTTGG TCATCACTGG TTGTTGGTCA TCACTGGTTG TTGGTCATCT 360 ATGTCACCTA ACAGGCCACT CATGACGTTA GCCCTTGACT TCAAAAAGGA CCTCAAAGAA 420 AATTCCAGTT TTCACTCCAA AAGGAGAAAT CAGGCCGAGC TGTGATGGCT CATGCCTGTA 480 TTCCCAGCAC TATGGGAGGC TGAGGCAGGC GGATCGCTTG AGCCCAGGAG TTTGAGACCA 540 CCCTGGGCAA ACCTATCTTT CCAAAAAAAT ACAAAAAGAT TAGCTGGGCA TGGTGGTGCG 600 TGCCTGTAGT CTCAGCTAGT CAGGAGGCTG AGGTGGGAGG ATCACTTAAG CCTGGAAGGT 660 TGAGGCTGCA GTGAGCGGTG ATGGTGCCAC TGCACTCCAG CCTGGATAAC AGAGCAAGAT 720 GCTGTCTCAA AAACTAGCAA ACGAAACAAA AGGAGAAACT GCTGGCAGCC CCTAATCTAG 780 TACTGTCCCG GCTCCACCCA CCTTCAGATC CAGCCTCCTC CCCTGGCACA CGGGAGCCCC 840 CTCCTCTGAC TGTGCTGAAA GTGAGGGAAG ATCCCCTCTG GGGAGAGAGC TGTAGCCTTG 900 ACCTCTGCAC ACCTTACTTA TCCAGAGCAC GAGGCAGGGC CGCTGACTCA TCCTGGTTTA 960 CCCTGGGCTT TCCCAGTTTC AGCACTGAAA GTCCCGCATC TGGAAAAGCC CCTGAGTCGC 1020 TGACAAACCA GACAGTCCGG ACCATGCAAA GCACAGTGCA TGGTGCTTTA GCCACAAAGT 1080 TGATTGAAAA GTCAGAGGCA GTGAGCCACA GGAAGCGCCA CGTGACCCAG ACTGCGAGGA 1140 GGACACAGGA AACCAACCCT CACTGTGTCC TGCTAGGGGG TTAACCCGTC TACAAGCATC 1200 AGGGTTGCCA TTTCAGAGAT CAGCAAACTG AACAGCAGTC GTGACTTGTC CTCGCCTGCA 1260 AGACAAGCGA GTAACAAATC CATGAAGGGA AGGACACGGA ATTGAGCAAG GGGGCAGGGC 1320 CGGATGTCAT TTTGGCGTTT TTTTTTCTTT CAGTGATTGA GGTAAAATTC ACATAACATA 1380 AATTAACCAT TTTAAAGTGT ACGATTCAGA GGCATTTGGT ACATTCACAC TGTTGTGCAA 1440 GCACCACCTG TATCTCGTTC CAAAATATTT TCACTTCCCC AAAAGGAAAC TGTGTCCCCA 1500 TCAAGCAGCC ACACCCTACT CCCTCACCCC CGCCCCCAGC CTCTGACAAC CACCAATGTA 1560 CCTTTTGTCT CTATGGATTT GCCTTTACTG AACAATTCAT AGTAATGGAA CCATACAATA 1620 TGTAGTCCTT TGCGACTGGC TTTTTTTACT CAGCATCAAT TTTTTTTTCT TTTTCTTCGA 1680 GACAGAGTCT TGCTCTGTCA CCCCGGCTGG AGTGCAGTGG CATGATCTCG GCTCACTGCA 1740 ACCTCCACCT CCTGGGCTCA AGCGATTCAC ATGCTTCAGC CTTCTGAGTA GCTGGGACTG 1800 CAGGTGTGCA CCACCATGCA TGGCTAAATT TTTTTTTTTT TTTTTTTTTT TTTTTTTTTT 1860 TTTTTTTTAG AGAGGGAGGT CTTACTACAT TGCCCAGACT GGTCTCAAAC TCCTGGCCTC 1920 AAGCAATCCT CCTTCCTCGG CTTCTCAAAG TGCTGGGATT ACAGGCTTGA GCCATCACGC 1980 CCAGCCTATC ATCCTAGTTT TGTTTTTTGG GTTTTTTGTT TGTTGGTTGG TTTGTTTGTT 2040 TGTTTTTGAG ACCTAGTTTC ACTCTTGTCA CCCAGGCTGG AGTGCAATGG TGCAATCTTG 2100 GCTCACTGCA ACCTCCGCCT CCTGGGTTCA AGTGATTCTC CTGCCTCAGC CTCTCAAGTA 2160 GTTGTGACTA CAAGCATGCG CCACCACACC TGGCTAATTT TTGTATTTTT AGTAGAGACA 2220 GGGTTTCACC ATATTGTCCA GCCTGATCTC AAACCCCTGA TCTCAAGTGA TCCTCCCACT 2280 TTGGCCTCCC AAAGTGCTGG GATTTCAAGT GTGAGCCACC GTGCCCGGCT 2330
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