Tag | Content |
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EnhancerAtlas ID | HS133-03480 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:212657770-212660340 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr1:212659447-212659458 | GGGTGACTCAG | + | 6.02 | JUNB | MA0490.1 | chr1:212659447-212659458 | GGGTGACTCAG | + | 6.02 | MAX | MA0058.3 | chr1:212659946-212659956 | AGCACGTGGT | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr1:212657998-212658013 | TGAACTCTTGACCTA | - | 6.21 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_35302 | chr1:212655268-212663203 | HeLa |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr1 | 212658172 | 212658571 | chr1 | 212659054 | 212659720 | chr1 | 212659085 | 212659948 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I212481 | chr1 | 212655167 | 212663350 |
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Enhancer Sequence | CTAATATGTT ATTCTTTTTT CTTTTTTGAG ACAGTTTCAT TTTTGTTGCC CAGGTTTGAG 60 TGCAATGGCG TGATCTCAGG TCACTGCAAC CTCTGCCTCC CAGGGTTCAA GTGATTCTCC 120 TGCCTCAGCC TCCTGAGTAG CTGGGATTAC AGGCGCCCGT TACCATGCCC AGCTAATTTT 180 TGTATTTTTA GTAGAGACGG GGTTTCACCA TGTTGGCCAG GCTGGTCTTG AACTCTTGAC 240 CTAAGGAGAT CCACTCACCT CAACTTCCCG AAGTTCTGGG ATTATAGGCG TGAGTCACCA 300 TGCCTTGCCC TCTGTTATTG TATTCTGTGG ACTTTTTAAA GAATGCTCAC CCCACCTACT 360 AAAGTGACTC CATGACCCAC TTATGGGTCT TGATCCACAG TCTGAAGGGC ATTGCATTAG 420 GGCCAGCCCA GGGCGAGTGG CCTTAGCTGG GCTGGCTATA GCGTGTAGCA GAGGTCAGTA 480 TGGAAAATGG CCCTAGGTGC ATTCTGGGGC TCCCCTTGGG GAAGGTTCCT CTTGTGGGGG 540 GTTCCCTAGA GGGTATTTCC TCCCTGTAGT CATCACATTC CAGGGGCCAG TTTTCCACTT 600 TGTAGGCCTA GAAATCCAAG TTGGTTAGGA GCCTTGGAGG TGGCTGAGTT GAGGGGTGAC 660 TCACACTGCA GCCCAAGTGT AAATATCAGA GTGCTGATTC AGTCGCTCAC GGTGAGGATC 720 CAGCTACCCA GTGGGCTGTG TTCACCCATC AGCACCTGTT CTCCAGTAGG GAATTCTACC 780 CAGAAGTCCA AACTGTCATC AGAAGGTGCT TGGCCAGCAC AGTCCTGGAG CAAGGGAGTT 840 AGGAGAAGCC CGGAGATACC TGCTGCGCAC CTGGGAGGCC TGAGCATCTC TCCGGGATAC 900 TCTCGAAATG CCTGCCTCCC GGCCTCCTTG GTCCTCACCA CCTGTGCTGA CCCACCTCTT 960 TGGCTGACCT GTCAAATCTC TTGTTCTGTC CTCATCTATG TCTGCACAGT TGAAGCTTTC 1020 TATTTCAAGT TCTGGTGGTG GGCGATGGGG CTGGTTGTGT GCATGGTGGC CTCCCATGGC 1080 TGCCCTGCAG GTGAGGTGGG TGGCACATGT GTTGGGGGAG TAGCAGGAGC TCCCTCTGAT 1140 TTACCTTCAG GTAGTCCAGA GATGTGTGGC CAGGGTCTAC TCATCAGCAA TAACCATACG 1200 CGGCTCTTTA TTGAGTGCTT TGTAGAATGC TGGGTACAGT GCTAAGCACT TCACTGGCAC 1260 TCTCATTTCT TTCCCATAAC CATCTGATGA AATAGTACTA CTTTCCCTGT TTTGTGCATA 1320 AAGAGATAAA GGCTTAGAGA GGTCAAGTGG CTTGGCCGAG GTCACTGAGT AAGCCAGTCG 1380 ACAGGTGGCC CTAGAAACTG TCTGTGAATA TATATGTGTG CTCTGAAAGG ACAGGGACCA 1440 TGCCTCCCCA TAAGCTCTGA CTCCCTAAGG GTAGGACTGT TCCCCCCTCA GTAGCTTCCC 1500 TCCCCACCTT GCTAGCCTCC CTGAAGTGCC CAGGGCAACA TGTGGCACAG CAGGGGTGCT 1560 CTGTTGCATG CTTGCTGACA GTCACGGACA GGGGACCAGC CTCTTGCCAA AGAGAGAAGG 1620 CCTGTGGGAG CCTCAGACCA CAGAGGAGTG ACTGCGTGGA TGCACCAGAC CATGGCTGGG 1680 TGACTCAGCG GCTGGCTGAC AGATGGATGA ATGGACGTCA GTCCTATGGT GTGGCCCTTC 1740 CCTTTTCTCC CCGGAACAAT AACACATCCT GGCTCCGTGA TTTCGTCGCC ATAGGAACTG 1800 GAAAACATTT GATAACATGG AGCCTCTGGG ACAGGTGGGC TGAGCAGGTC TGAATAAAAA 1860 CAACCCTTTC CTGCCCCTTC ACCCAGAATC CAGGCATCTG GTCTATTTGC AGCAGGTTAG 1920 GTAAATAGCC TGGGGGGAAC CATGCAGCCA CCTGAACTGA CCGACCTTGT CCAAACTAGG 1980 AAGTCAGGGA AGTCACTGTC TATGCTGGCA GGACCTGGCA CAAATTCCTG GTAGGAGGAA 2040 ATGGGGCCTC AGGCACCCTG TCTGGACATT CTGAGTATCC TATGGTGTGC CTGTCCCCAG 2100 CACATGTGGG CTCTGTCCTG GACACTGTGG GGAATTAGAA GAAGGAAAGA AGGGGGACAG 2160 GGCTCCAGGC TCAGAAAGCA CGTGGTCTGC TAGGGGGCAG GGCACATATA GAAACAGTCC 2220 TATTAGGTCC CAGTCCTAGC ACAGATGGGG AATTACACGG ATCAGTAGGG AAGGAGTTGG 2280 GAGGTAGGTT CTGGGAGGGG ATGGGGTTTG GTGGAATGGA CCAGAATTCT CCATTCCCCA 2340 GCAAGCCCTA ACCAAGTGTG GCACCGTGCT CACATGCACA ATCTGGGTCC TGGGGTGACT 2400 GCTGGGGGCC AGGGCACTGC ATTCTCTTAC TGGCTTGGCC GTCTCAGCCT TCTCTGCCTG 2460 ATGCTTTTTG GTTCTACGGT CCTTGCTTTT ACTCTTCCAG TGCTGTTGGG CACTTTCTAT 2520 GTAGGGCACT TGACTTGGAC ATCTTTTTTT TAAATTTTAA TTTAATTTTT 2570
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