Tag | Content |
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EnhancerAtlas ID | HS133-18174 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr2:224806120-224807620 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr2:224806163-224806181 | GCATCCCTCCTTCCTTTC | - | 6.06 | EWSR1-FLI1 | MA0149.1 | chr2:224806127-224806145 | CTGTCCTTTCCTCCTTCC | - | 6.17 | ZNF263 | MA0528.1 | chr2:224806123-224806144 | CCTCCTGTCCTTTCCTCCTTC | - | 6.41 | Zfx | MA0146.2 | chr2:224807178-224807192 | CCCGCCTCGGCCTC | + | 6.01 | Zfx | MA0146.2 | chr2:224807495-224807509 | CCCGCCTCGGCCTC | + | 6.01 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_61356 | chr2:224803424-224831902 | HBL1 |
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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 | TTCCCTCCTG TCCTTTCCTC CTTCCTCTGC CTGGGATGAG GGTGCATCCC TCCTTCCTTT 60 CTAGATGCCA CTCCTCTATC CATGAAGACC AGCTCAACGA CCTTCTCTAG GAGGCTGTCC 120 CCAAACCCCG GCCCCAGCCC AAAGAGCCTC CTCTTCCTGT GTCTTCCCAG CACTGGATGC 180 TGAATACATA GGGGCCATCT CTTCACTAGA CTGTTCAGCC CTTGGGAAAG AGCAACTTAG 240 CTGTCAGCTG TCTCTCCCCC ACAGGTCTAG CATGGGCCCC ACACACGTGC TGGGATTACA 300 GGCGTGAGCC ACCTTGCCTG GCCAAGGTAG TGTGGCTTTT GACCCCTGTT GTGTCCTCAG 360 GGCCTGACAC TCAATAAAAA AGCTTTTTCT AAATGAATGA GTAAATGAGT GAAGAACGTG 420 ACACGTATTT ATGACAATGT GAAAACAAAC CACCATGGCT AACACCAAGA AAAAACCCAC 480 GCCCATGTGC TTTCATTACA TCTCATGAAG TGTAGCACCT ACTAAAAAGG TTGTTCTCCC 540 TTCAAGGAAG TTGCAAGAGC CTGAACACAA CAGAAACCTC AAACGCCAAC CCCATCCTGG 600 TCCAGTCATC TACCTGGGCT CTGCAATAAC AGTGGTGCAC GAGTGAAAAA GTGAGCAGAT 660 GCAAGCTCCC CCAGAACGTT TCAGTCCCAG AGCAGCTTAG TAATCACTTT CCAAAAACAT 720 TTATCAGCAC TGCTCCTGAC CAGCAATCTC AAATATTTAG CAACTTACCC AAAACGCATG 780 ATTCATGAAT AAAATATTTG ACCGAATAAA GGCTGCTAAC TTTTTTTTTT TTTTGATACG 840 GAGTCTGGCT CTATCGCCCA GGCTGGAGTG CAGTGGCACA ATCTTGGCTC ACTGCAAGCT 900 CTGCCTCCCA GGTTCACGCC ATTCTCCTGC CTCAGCTTCC CGAGTAGCTG GGACTACAGG 960 CGCCTGCCAC CACACCTGGC TAATTTTTGA ATTTTTAGTA GAGACTGGGT TTCGCCGTGT 1020 TAGCCAGGAT GGTCTCGACC TCCTGACCTT GTTATCCACC CGCCTCGGCC TCCCAAAGTG 1080 CTGGGATTAC AGGCATGAGC CACTGCGCCT GGCCAAAGGC TAACTTTTTT TTTTTTTTTT 1140 TTTGAGACGG AGTCTCGCTC TGTCGCCCAG GCCGGACTGC GGACTGCAGT GGCGCAATCT 1200 CGGCTCACTG CAAGCTCCGC TTCCCGGGTT CACGCCATTC TCCTGCCTCA GCCTCCCCAG 1260 TAGCTGGGAC TACAGGCGCC CGCCACCGCG CCCGGCTAAT TTTTTGTATT TTTAGTAGAG 1320 ACGGGGTTTC ACCTTGTTAG CCAGGATGGT CTCGATCTCC TGACCTCATG ATCCACCCGC 1380 CTCGGCCTCC CAAAGTGCTG GGATTACAGG CGTGAGCCAC CGCGCCCGGC CCAAAGGCTA 1440 ACTTTTAAAG AGTGTTGTCT GCATCTACGT TCACATCATG CAAGAGTCAT TATTCTGGCC 1500
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