Tag | Content |
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EnhancerAtlas ID | HS002-06307 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr21:34754690-34755920 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
USF1 | MA0093.2 | chr21:34755676-34755687 | GCCACGTGACC | + | 6.62 | USF2 | MA0526.2 | chr21:34755674-34755690 | GCGCCACGTGACCCAG | - | 6.69 |
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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: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH21I033378 | chr21 | 34751108 | 34757769 |
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Enhancer Sequence | CAGAGAGGCC CAGTCGCTCT TCTCAGAGTC TCCGTGGCAT CTCGGTAGAT TTGCTGATCC 60 CTTTACATAA CCCAAGTTGA GGCATGCCCT AATTTCACCC ACAAATGCTA CTAAGCCCAG 120 GCCCTTATCC AGCCAAAACC ATCCTGCCAA GCTCCCACCA CCACCATCAG CATCATTTTC 180 AGGTTGTTGG TCATCACTGG TTGTTGGTCA TCACTGGTTG TTGGTCATCT ATGTCACCTA 240 ACAGGCCACT CATGACGTTA GCCCTTGACT TCAAAAAGGA CCTCAAAGAA AATTCCAGTT 300 TTCACTCCAA AAGGAGAAAT CAGGCCGAGC TGTGATGGCT CATGCCTGTA TTCCCAGCAC 360 TATGGGAGGC TGAGGCAGGC GGATCGCTTG AGCCCAGGAG TTTGAGACCA CCCTGGGCAA 420 ACCTATCTTT CCAAAAAAAT ACAAAAAGAT TAGCTGGGCA TGGTGGTGCG TGCCTGTAGT 480 CTCAGCTAGT CAGGAGGCTG AGGTGGGAGG ATCACTTAAG CCTGGAAGGT TGAGGCTGCA 540 GTGAGCGGTG ATGGTGCCAC TGCACTCCAG CCTGGATAAC AGAGCAAGAT GCTGTCTCAA 600 AAACTAGCAA ACGAAACAAA AGGAGAAACT GCTGGCAGCC CCTAATCTAG TACTGTCCCG 660 GCTCCACCCA CCTTCAGATC CAGCCTCCTC CCCTGGCACA CGGGAGCCCC CTCCTCTGAC 720 TGTGCTGAAA GTGAGGGAAG ATCCCCTCTG GGGAGAGAGC TGTAGCCTTG ACCTCTGCAC 780 ACCTTACTTA TCCAGAGCAC GAGGCAGGGC CGCTGACTCA TCCTGGTTTA CCCTGGGCTT 840 TCCCAGTTTC AGCACTGAAA GTCCCGCATC TGGAAAAGCC CCTGAGTCGC TGACAAACCA 900 GACAGTCCGG ACCATGCAAA GCACAGTGCA TGGTGCTTTA GCCACAAAGT TGATTGAAAA 960 GTCAGAGGCA GTGAGCCACA GGAAGCGCCA CGTGACCCAG ACTGCGAGGA GGACACAGGA 1020 AACCAACCCT CACTGTGTCC TGCTAGGGGG TTAACCCGTC TACAAGCATC AGGGTTGCCA 1080 TTTCAGAGAT CAGCAAACTG AACAGCAGTC GTGACTTGTC CTCGCCTGCA AGACAAGCGA 1140 GTAACAAATC CATGAAGGGA AGGACACGGA ATTGAGCAAG GGGGCAGGGC CGGATGTCAT 1200 TTTGGCGTTT TTTTTTCTTT CAGTGATTGA 1230
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