Tag | Content |
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EnhancerAtlas ID | HS101-44414 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr8:141506220-141507480 |
Target genes | Number: 11 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr8:141506603-141506614 | CTGAGTCATCC | - | 6.32 | FOXA1 | MA0148.4 | chr8:141506824-141506840 | CTTTATGTAAATAAAG | + | 6.14 | Foxd3 | MA0041.1 | chr8:141507382-141507394 | GTTTGTTTGTTT | + | 6.32 | JUNB | MA0490.1 | chr8:141506603-141506614 | CTGAGTCATCC | - | 6.14 |
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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 |
GH08I140496 | chr8 | 141506119 | 141506884 |
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Enhancer Sequence | TCTCGATCTC CTGACCTCAT GATCCACCCG CCTCAGCCTC CCAAAGTGCT GGGATTACAG 60 GCGTGAGCCA CCGCGCCCGG CCAACAGGGC CTTTTCTTTT AAATCAACTT CATTATGACA 120 TAATTTCATA GAGTAAAAGG CATCCCTTTT AAGTGTACAA TGTAATGAGT TTTGACAAGT 180 GTATACACCC TTATAACCAC TTTCACAATC AAAATAGAGA CATTTCCACC CTGCCCCTTG 240 GCAGTCAGCC CCATCCCCAC CCTGGCAGGC AACCGGGGGT CTGTTTCCTG TCACTGTGAA 300 CGTGCTCAGC CTGATCTAGA ATTTCATGTA ACGCGGTCCT GCAGGAAGTG CGCTTCTGTC 360 TGGCTTGCCT CGGCACAGTG CTTCTGAGTC ATCCAGGCGA CTGTGTGTAC CCGTTGCTTC 420 TCCCACTGTT GGTGTTCCAT GCAGGGATGT GCCATGGTTT GTGAACAGTC TCTCTGCTCA 480 TGGGTGTTTG AGTTGTTTCC ACCCATAGTT ATCATGAATA AAGCTGAAAT GAACATTCAG 540 GGACAATCTT GTGTGGACAT ACCTGTTTGT TTCTTTGGGT AAATAACAGA AGTAAAGTTA 600 TTTACTTTAT GTAAATAAAG TAATTTATGG GAGTAAGCTG GCTCCCATGG TAAGAGGATG 660 TTTAGCTTTT TAAGAACTGT AACCTATTTT CCAAAGTGTT TGGAACATAT AGCATTGCCA 720 CCAGCAGTGT GTGAGGGCAG CAGTTGGGGC CACACCTCAC TCTCTAACAT GGGGTACCAC 780 TGCATCATGA GTCTTGTAGA GCGTACATCC TGGCTCCTGG CCCAGTGCTG GCCACTGTGG 840 GTGCCCATTC TATTTTTTTT TGAGACGGAG TCTCATTCTT GTTGCCCAGG CTGGAGTGCA 900 ATGGCGCCAT CTCGGCTCAC TGCAACATCC ATCTCCCAGG TTCAAGTGAT TCTCCTGCCT 960 CAGCCTCCCG AATAGCTGGG ATTACAGGCG CCTGCCACCA CGCCTGGCTA ATTTTTGTAT 1020 TTTTAAGAGA CAGGGTTTCA CCATGTTGGC CAGGCTGGTC TCGAACTCCT GACCTCAGGT 1080 GATCCACCTG CCTCGGCCTC CCAAAGTGCT GAGATTACAG GTGTGAGCCA CTGAGACCAG 1140 CCTTTTTGTT TTGTTTTGTT TTGTTTGTTT GTTTTTTAGA GACAGGGTCT TGCTCTGTCA 1200 CCCAGGCTAG AGTTCAGGGG TGCAATCACA GCTCACTGCA GCCTCAGACT CCTGGCTCAA 1260
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