Tag | Content |
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EnhancerAtlas ID | HS134-09766 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr11:31884580-31885860 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F6 | MA0471.1 | chr11:31885125-31885136 | GGGCGGGAAAG | + | 6.32 | FOXP1 | MA0481.2 | chr11:31885743-31885755 | CTCTGTTTACAT | - | 6.32 | FOXP2 | MA0593.1 | chr11:31885744-31885755 | TCTGTTTACAT | - | 6.02 | Foxa2 | MA0047.2 | chr11:31885746-31885758 | TGTTTACATTGG | + | 6.62 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 31884681 | 31885200 | chr11 | 31885200 | 31885409 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I031863 | chr11 | 31884634 | 31885730 |
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Enhancer Sequence | AATCTGTCTT TTTAAGCCAT TGTTACTTTA TTGTTGTTGG TGATTTTTTT TTGTTTTTTG 60 AGACAGGGTC TTCTTTCATC CAGGCTGGAG TGCAGTGGTG CAATCATGGC TCACTACAGC 120 CTCAATCTCC CAGGATCAAG CAATCCTACC ACCTCAGCCT CATGAGTAGC TGGACTACAG 180 GTGTGCACCA CCAAGCCCGG CTAATTTTTG TATTTTTTTG TAGAGATGAA GTTTCGGCAT 240 GTTTCCCAGG CTGGTCTCAA ACTCCTGGAC TCAAGCGATC CACCCGCCTC AGCCTCCCAA 300 AGTGCTGGGA TTAATGGTGT GAGTCACTGA GCCCAGCCTG CCACTGTTAC TTTGGCTTTT 360 GTAGGAGCCA ACTAACTGGT ATTCTAACTA GCACAGGTAT CATTGTTGAT TCTCTGGCAG 420 ACATATTTCA GAATTCCAAG AGACCAGATT TGTAGTGTTC TACAGGAAGC TGTGCTTTTG 480 TTTGCATTGA CATTCCTTTT GCTTATTCCA CAGCAGACAT GGAAGCAAGA CACAGGTCCA 540 GGATAGGGCG GGAAAGTGGC TTTCTCAGTG ACATTTCAGT GTGAATGAGA CTGACCCAGG 600 GAGTTTGTTA AAATGCAGAT TACTTAGCTC TCTCCTTTGG GATGTGAATT TGACAATTCT 660 GGCCTGACCC AGAGAATCAG CATTTGAAAA GTATTCCACG TCATTCTGAT GGCAGCCCTT 720 GGGCCACACT GAAAAAAAAA CTCTGGTCTA TAAGTGGAGC CCTTCAATAT GCGGGACTCC 780 TGGGAAATAC TTCAGTGAAT TAACTCAGGA AGATTCTTAA CTGCTACAGA GATGCTGTTG 840 ATGGTGGTGT TTAGCAGTCT AGGAACAGCG CCTTGGAAAT GAATACTTGG AAATATTTGA 900 TGGGACACTC AGTGAAATGC AGACATTTGG AAAGTTACAA AGCTTTACTC TGGATGGCCT 960 GTAAATACCA CACACATGCA CTAATTAGAT AACCAGACAT AATTAAACTA TTTGGAGACA 1020 TGATTGAAAA GTAAATATTT TAAGGGACAA GAGGGCAAAT TTTAAACACT CCATTCTTCA 1080 CGCTCATTTC TTTAGTTCAC AATGTTGACT GAGAAGTCGG GGTAATTACA AGTGGTAATA 1140 ATGCTTGATA ATTACATATT TGCCTCTGTT TACATTGGAC ATGAAATTAG GAAACTCACT 1200 TCCTAAGTGA ACCCTTGTGA GCATCCTTTC ACAGAGAGTG AAGTTCATAT CACAATCAAA 1260 GCAATAAGAG GGAGTAATTG 1280
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