Tag | Content |
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EnhancerAtlas ID | HS133-23671 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr4:1159810-1160720 |
Target genes | Number: 11 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EN2 | MA0642.1 | chr4:1160648-1160658 | CCCAATTAGC | + | 6.02 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_20277 | chr4:1159959-1167262 | CD56 | SE_41804 | chr4:1159880-1166321 | LNCaP | SE_65329 | chr4:1159993-1163945 | Pancreatic_islets |
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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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Enhancer Sequence | TGTCAGTCCC AGGAACCTTA AGAAAACTTT AAGCCAGGGG TTTTTCAGAT CTCCACGTCA 60 CCTCAGAGCT CATGCGCCCG TGAGCTTGGG CTTAGTTCAT TGTTTTCAAG GATGGTGGGC 120 GGGGATGGCG TGCAGGGTGG TGGGAGCTGG GCCTGGGGTC TGGTTCTAGA AGCATCAGGG 180 CTGGAGGGCC TTAGACAGTT ACGAGGAAGG GTCGTCTACC AGGCCTCGGT GAGAGAAGTG 240 AGCCCCCACC TTCCAGTCAC TGGGAGAGGA CTGAAGAAGC AGCCATCCCC CAAGCATCTC 300 CATCCTCAAA CCACACAGAG CTCCCGCCCA GGCACTGAGA GGGCCCTGGG GTTCCACCAG 360 GTGAGTGGCA CTGGTGGGGA GGCCTGGGGA CCCCTGCTGC AGAAAGGGCC ACGACAGATT 420 ACAGTGAGCC CCTGAGGACA TCTTTGAGGT TGGGGCCTCT GAGCTCAGGT CTCAGGAGGT 480 GTCTGCTGGT GGCCTGATGG GCTGCGAGGG TCTTGGTGGT CAGTGGCCCC CCCATGAACA 540 GCAGCAATGC AAGCTGCTCC CACAGAGGAG GGGGCAGAGT GAGGGCTTCT GGGGCCTCGT 600 CCGGATCTCA AGGTGCCCCT TGTCTGAGCT TCTGATCGTC CTGTGGGCAG GCGCGTGCCT 660 GCCGGGTTTG TGGATGCATC TGACATGCCA TTTGCTGTGT CTTCTGAAAT CCTGTATGGG 720 CCAGGGGTGG CGTCTGTTGT GGGGAGATCT GTAGGTCTCA GGCCTGCCTC CCACACACAC 780 ACAGAGCACG TGCCTCATGG CCCTGACGGC AGCACCAGGC GCCTTCTGAA TGTGTGTCCC 840 CAATTAGCGC ACACCACGGG TCCCTGCACT GCACGGGGCC CAGAACAAGT GTGGGGACAG 900 CCAGGGACAT 910
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