Tag | Content |
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EnhancerAtlas ID | HS133-02602 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:156870840-156872300 |
Target genes | Number: 26 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr1:156871667-156871687 | TGGGAGGGGATGGTTTGGGG | - | 7.96 | ZNF263 | MA0528.1 | chr1:156871653-156871674 | GGAGCAGGGCAGGGTGGGAGG | + | 6.18 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_38284 | chr1:156862281-156872673 | HUVEC |
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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 | GGCAAAGGAT GGTCAAGCCA AAACCTTCCT CTTCCTGCCA GGACCCCCAT CTCATCTGTC 60 CCCTCCCGGG GCCACCCACT GATCTCCCCT GACCCCACCC TGGCTTCCAG CCCCTGGGCT 120 GACCAGCTGA TGCCTCCTCC GCACTCTGGC CCTACCCTGA GGACCTTTGG GAAAACAGAA 180 CCTACCCACC CTTCCAGCCA GCTAACCTCC CAGCCAGCCA GAAGTGGGTG GGGATGAGAG 240 TCAGCTCCTC CTCATGCTCC TCAGTCCTTC AGTCCATCTC AAAGTCCCCC AGGTGAACCG 300 TGTCCTCTAG AAGTTGGCTG GGAGGAGGTG ACAGGGACAG GACTTGGGTG GGTAGGGGCT 360 GACAGGAATG GGAGGAAGGA CCTTTTCTCG GCCCAACAAC AGCTCAACCT ATATGGCACT 420 TCCTCCCTGG GCCTTAACTC GACTCCTTCC TGCAACAAGT TTTGTCCATG CCACCACGCC 480 ATAGGCTCTG TGAACAGATC CAGGGCAGAA GGATGGCTGG GGAGTCCTTG TGTGTCTCAG 540 GAGATGAGGC TCACCCAGGG ACAAGGGTGA TGAGCCTGGC TTCAGACAGA CTGAGCTGCA 600 GTTGGAGCAC AGGGGCCCCA CGCCAGGGCC AGAGCTGAGG GTCAGGGAAG AGGGGAGTGT 660 GGAGACCGAG AGATGAGGCA GAGGCATATG GAGGGCTCGG GGTCCTGACC AGGGCCCTGG 720 CTGCCAACCA CACTGAGGGA GAGGTGGAGA GAAGGTTAGC TGGGGCTAGG CAGAGCGATC 780 CCTGGAGTGG GCATTGGGCC TGGGAAGATG GCTGGAGCAG GGCAGGGTGG GAGGGGATGG 840 TTTGGGGACA TTGGGAGAAG GGATGACTCT ATTTGGGAGT GGGGATGTGT CTGGGTGATG 900 TGGGGGTGGA GCTCTGGGAC AGACTCTGGG GAGTGTCTCT AGGGCACTCC TGACTGTGGC 960 CTCTCCCCTT CAGAGGGGGC CACAGTGTCA GCTCTGGAGA CAAGCTGCCA GAAAGAGGCT 1020 TCTGGTCATG GCCCTCCCGT ATGCTACCCA CTGCGTTCAG GATGGTGGGA GGATGGAGCC 1080 ACCCCCGTCA CGCTCCCTGC TGTCCCCCTT CCTAGCCAGG CTCTGTTTCC TGTTTTCAGG 1140 CTTCATATCC TGAACGCTGG GATCCCCCAG GACATTCCCT GGCCCCCAGG CCCCAGGTCC 1200 CAGGCCCCAG GGCTGAGCTG TGGGCAGGCC CCACCTGGTG AGTTACTTGG GGACTGAGGA 1260 TGGATAGGAG GAAGCACAGA GGAGGCTAGA GGCTGAGATT CGCCCTGCGG GAAGTGTGAT 1320 GGGGCATGCG GCTGGGCTGC ACTGGAGGGG TGGGTAGACG CTGGCACTGG GAGGATAGGT 1380 GGGCCAGCAT CCTGGATGAA AGGCTGGAGA TTTGGCTGCT GGAGGGTTAA AGGTGAAGGA 1440 GGAACATGGG CGGCTGAGAT 1460
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