Tag | Content |
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EnhancerAtlas ID | HS133-20661 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr21:44264000-44266230 |
Target genes | Number: 12 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr21:44264400-44264420 | CCCCAAAACACACACACATA | + | 6.37 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr21 | 44265477 | 44265779 | chr21 | 44264521 | 44264614 | chr21 | 44264671 | 44264783 |
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Enhancer Sequence | GTATTGCCCA GGCTAGTCTC AAACTCCTGG GCTCAAGCAA TCCCCCTGCC TCAACTTCCC 60 AAAGTGTTGG GATCACAGGT GTGAGCCGCC AGCCTAGCTG GAAGACATTT TTTTAAATAC 120 CAAAACCAAA TTTATAGAGA TGAAAAAACA CAATGGCTCA TACAGAAAAT GGCCATAGCT 180 TAACAGCAGC TTAAAAGATC AGTGGGCTTG AAGACGTGGA AACAGAATCT ACCAAAAATG 240 AAACGCAAAC TGAAGAAGAT GAGCAGACTC ACGGACCCAT GAGTCCACAG CAAGCAGCCC 300 ATTCGAGTAC CTGGGACTGC AGGAGGCAGG GGAAGAGACC GAATAGCTAG AATATTTCCA 360 AATTGCATAA AAATGACAAA GCCTACAAAT CTTGACAAAC CCCCAAAACA CACACACATA 420 CCCTAAAGCT TATCAAATTA CAGAAAACCA GGGATAAAGA GAAAAAAACA AAAGCAGCCG 480 CAGAATACAT ACATGATGAC TATCATGTAT CAGTCAAGAG ATAGAAACAT TTAACACGAA 540 GAATGATTCA ACAGGAACAG AGGGTTCCAC TAACATGTAA AGAGACTTCC GAGAACGGAG 600 GCGCTGAGGC CTCGGGAGAA CCTCCACCGC CAGGACTGAG ACAACAAACC CACAAGCGTT 660 GAGTCTGGAT CTTGGTGAGA ACCTCGGAAC CCCACGTCGG CTGAGACGCA GCTCTGACCT 720 GAGTGGGGCT ATGATGTGCC GGGTGGTGCA GTTGGCCAAG GTGCAGCAGG CCAAGGCCTG 780 AGAGCAGGAA GCCCGGGGCA GGAGTGCCAG CGAGACTCAC CCAGAAGCTC TCCCTGGGGC 840 AGGAGGGAGG CAGACGCCCT GGGAGCTGGA CAGAGGCAAG GAAGCTTAGC AGGAATCCTT 900 CCCACCGTGG TGAATGAACC TGGGTGTTGC TAAACTCCTG CAGACTGTCA CTGAGAGCCC 960 CCGCCCCCAC CATGAGGCTG GCAGGCACAC ACCACGGAAG CCAGGAAAAG CAAGCACACT 1020 GGAACCAGGA GGGCAGGCCC CTCCCTCCTG TGGAGTCCCT CCAGCTCCTT CCAGTGACAG 1080 AGCCAAACAC TGTGCCAACC TGCAAAGGAG GGTACAGGGA GGGCCCAGCC CAGGGTCACA 1140 CGGCAGGGCT GAGAAGGGTG CACTGGGCAC GGAGAGGCAA GACACGGATA GCTGGAGATA 1200 CCGTGTGGGG GCCACACATA TCTGCACGTG CACATACAAT CACCCTCCCA CTATGAAGCA 1260 CAAAACAGGG CTCAACAAAT CTAAAGAGAG GGAAGTCAGC AAAGTATATT CTGAGACCAC 1320 AGTGGAATTA AAACCAGAAA CCAGAAACAA CAACAAAATC TGGAGGAAAA CCCTAAATGT 1380 TTGGAAATTA AACCATACTT CCAAATAACC CACAGACCAA AGATCTCACA AGGGAAATCA 1440 GAAAGTAAAA CGTATCACGT CAACATATAT GGGGTACAGG AAGAAACACA GAAAGCTCTC 1500 CTTCCCGGAG GGGCCCTCGC GGCTGGTCAG CTGCTGCTGG CTGCTGGCAG GAGGCCTCAG 1560 TTCTCTGCCA TGGTAACCTT TGTAGGCTGG CTGAGTGCCC TCGTGAGCTT GCGGCACATT 1620 TCCCCCAGGG TAAGTGATCT AAGACGGGTA AGTCAAGGTT TTGGTAAGGT GGCCTCAGAG 1680 AACAGGATCA AGGTTAGGTC TGGATCGAAG GTGGGCAGTG TCACTGGCTC CCTGCAAAAC 1740 TCCACACCAC ACACTGTGGG CCTTCCAAGT CGATCATGAG CCGCCACAGC CGCAAACACT 1800 AGGCGTTGAG GATGCACTGC GTTTTCCACG CTGGGGTCGG GGTCTGGGAT GAAGGACTGG 1860 CAGGATCTTC TAAGAAATGT GCATAACTGA GAGCCAGCAA TTCCACGCGC AAGTACACAC 1920 CCAACAGAAA TGCTTACAAA TGTTCCAGAA GACGGGTGCT GGCCGGGGGC AGTGGCTCAC 1980 ACCTGTAATC CCAGTGCTTT GGGAAACTAA GGCAGGAGGA CTGCTTGAGG CCAGAAGTTC 2040 GAGACCAGCC TGGGCAGCAG AGCAAGACAC CATCTCTACA AAAACTACAA AAATTAGCCA 2100 GCACGCAGGC ACACACCTGC AGTCCCAGCT ACTCAGGAGA CTGAGGTGGG AGGATCGCTT 2160 GAGCCCAGGA GGCCCAGCGA GCCAAGGTCA CACCACTGCA CTCCAGCCTG GGTAACAGAG 2220 CAAGACCCTG 2230
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