Tag | Content |
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EnhancerAtlas ID | HS182-20802 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr8:42122340-42123820 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr8:42123319-42123330 | GGGTGACTCAG | + | 6.02 | JUNB | MA0490.1 | chr8:42123319-42123330 | GGGTGACTCAG | + | 6.02 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_26990 | chr8:42122587-42124433 | Esophagus | SE_34968 | chr8:42122667-42124204 | HeLa |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH08I042264 | chr8 | 42122049 | 42125756 |
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Enhancer Sequence | TGCTGGGATT ACAGGTGTGA GCCACCATGC CGGGCCTTAA ACATTTTTTT TTTTTTTGAG 60 ATGGAGTTTT ACTCTTGTCA CCCAGGCTGG AGTGCAATGG CGCCATCTCT GTTTACTGCA 120 ACCTCTGCCT CCTGGGTTAA AGTGATTCTC CCGCCTCAGT CTCCCGAGTA ACTGGGATTA 180 CAGGTGCTTG CCACCACGCC CAGCTAATTT TTGTACTTTT AGTAGAGATG GGGTTTCACC 240 ATGTTGGTCA GGCTGGTCTC AAACCCCTGA CCTCAGGTGA TCCACCCCAC TCGGCCTCCC 300 AAAGTGTTGG GATTACAGGC GTGAGCCATC GTGCCCAGCC CATTTTATTT TCTAAGTAAA 360 GATAGGTTCT TGTTATGTTT CCCACGCTGA TTGTGAACTC CTAGACTCAA GTGATCCTCT 420 TGCTTCAGCC TCTGGGATAG ATGGGACTAC AGGTGCACAC CACCACACCC GGGCAAAAGG 480 GTCATTTTTA TTCTGCTTTC GGAGTTGCTT CTTCGGTTGC TGTTTCTCAG AATAATCTGT 540 ATGCCAAAGA GGCCTATTTT GGGTGGCATA TTCTGGTCTC CTACTGTGAT CTGGCCTCCC 600 AGATAGTCAC CAGCAGACTC CTGCAGAAAG GAAAAGTTGG GACAGGCAGG TAGGAGGGCC 660 AGGCACCACT GACAAGGGGA AGTGCAGAGA GAGGCCTGAG CCCAGGAAGG ACTAGAGTCC 720 GGCAGCTGAG CTGCAACACA GCCCATGGGT CAAAAGTAGG AGCTCAGAAC CAAGGTAAGC 780 CGAAAAGCAT ACCTGTTGGT TTCTTAGACG TCTACACCGG CCCATAGCCT TTGTCTCCGC 840 CACCATGGCC TGAGGTGGCA GCTGCCCTTT CATGACTTCT TCCTCTTTAG TTTGAATTTA 900 CTGGAATAAA AACGTGTGTG TAAAAGTAAA GGGAGCTTAA AAAGTGATTT CCTCCTCTAA 960 GCTCTTGTTC CTCCAGAGAG GGTGACTCAG AGCCCCAAAT CCTTGCCTTT GCTTGTTTCT 1020 GCCTAAGTTT GAGGCACAAC AGCCGGCTGG CCCTGCTCCT CTCAGTTTCT TGATTGGCCC 1080 AGGTCCAGTC ACAGAGACAG CAGCTGGCCA ATTTCCTTTC CTTCCTCTTC TGCAGCCAGC 1140 TCTGCATGGA GCCCAAAGGG TCTGCGGCAA GGTTCATTCT CACCCTCGTC TCCACCAGCC 1200 CACCCTCATC TCCCACCAAG GTCCCCAGAA CAAAGGCAGA CTTCTTCACA TCCTCCGACT 1260 TTCTAAACTA GTTTCTCCAA CTTTTCTGGC AGAGGAGTTT TTGTCTGTTG AAGAAGCAAG 1320 TCCTGACCTG CAGAGTCCTT TCTCTGCAGG GCTGGGATAA AACAAAATCA GATGGGTCAT 1380 GAAAGAGTTG CTGAAATCGC TGAACCAGAG CTGACTATGG GGGCTGGGGT GCTGGGGAAA 1440 TCCTCCCCAT CCTCTGTGGT CTGCCTTACG GCCTCTTATC 1480
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