Tag | Content |
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EnhancerAtlas ID | HS076-11754 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr11:116686740-116689020 |
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) |
Foxd3 | MA0041.1 | chr11:116687337-116687349 | GTTTGTTTGTTT | + | 6.32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 116687094 | 116687347 | chr11 | 116687011 | 116687285 |
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Enhancer Sequence | CCTGGTCAAC AGCTAGCATG CACTGTCAAT GACATTCTCT CTTTCAGAGG TATTCTAGGT 60 CTAACTGTTA AGCTAACAGG ATTTTCACTT CCTTACACGT TCACATACCA ATATGTATGT 120 GTGTTCCTTG ACCGGGTTGT AAAGTACATA ATAGTTGAAA CCTTGCTTTT TTTTTTTTCA 180 TAAAATATCT TGGACATCTT CCCATAAATA AACAGATTCC CCAAACCAAA CCAGAGTGTT 240 TTGCTTGAAC TCAGGACCTC ATGAGAGATC TGAGACCAGC TGTTAGAGAA TCTCTGAGAA 300 GGGCAGGTAG AGGCTGTTGC CCAGGTCCCC AGTCAGCTCA GCCGCTGGAG AGGAGCAGAG 360 GACTGACTGG CCACAGGGGG ACTAAGTCCA CCTGCTAGCT CAGAACAGGA GGAAGGCTGC 420 TTTCCTTGGA AGATGGGACC AACCCTAATG AGGACTAATA AGTGTATCTC AGACAAACCA 480 ATTGACCAAC TGGAACAGGC CAGAGATGAG GGTGTGTCTT CCAAGGCCCA AAGCAAGAGA 540 AACATCCCTA AGAGGGAAGG GGTGTGTGGG GTGTGTCAAT CAAAGTGATG TGTGTGTGTT 600 TGTTTGTTTT TGAGACAGAG TCTTGCTCTT TCACCCAGGC TGGAGTGCAA TGGCCTGATC 660 TCAGCTCACT GCAACCTCCA CCTCCTGGGT TCAAGCAATT TTCCTGCCTC AGCCTCCTGA 720 GTAGCTGGGA TTACAGGCGT GTGCCACCAC ACCTAGTTAA TTTTTGTATT TTTAGTAGAG 780 ACGGGGGTTT CACCATGTTG GTCAGGCTGG TCTCGAACTC CCTATCTCAG GTGATTCACC 840 CACCTCAGTC TCCCAAAGTG CTGGGATTAC AGGCGTGATC CATCACGCCT GGCCTCAATC 900 AAGGTTTTTA ATTGCTAGCC ACAGAAACCT ACTCTGGAAG ACATAATCAG AAGATGAACT 960 TACTGACATA TTTCCAGGAA TTTCAAGGAA ATGTCTAGGA AAGCTGGAGT ACTTGGTTTG 1020 GAAAATAAAC AAGAATAAGG GGAGCTGAGG GAGAAACATG GCCATGCTCA TGCCACAGAA 1080 CTAGAGTGAT GGGGACGGCT GTGCTGTCAC CACTGAGCCA GGATGGGGAC AGCCCAGTTT 1140 GCCCACCAGC CACTGCCACG CCTGGTCCCT GGCCTGAGGC TCTAGCCTGG CCGCAAGCTG 1200 CCTGTTGCTG CCGCACTGTT CCTGCCCACC CCAGAAAAGA TTCTCCACTG TCTCTGTTTC 1260 TTTACACCAG TCTGGGGCAA TTACATCTGA TTTGCTGAGC ATAGGTCCCA TGTCCCATGC 1320 TGGAGGTAAG CGAGGCTAGA AGGCAGGCGA CTGGAGTTGT TAGTGTCTGT AATGGAGGCA 1380 GCCTCTGACT CCCACCAAAA CTCATCAGCG AGACACTTTC GAAACAAAAC AGGAGAGCTT 1440 CAGAGGCTGG GAAAGTGTCT TAGATCTTTT GGGCTTCTAT AACGAGACAC CAAAAACTGG 1500 GTGGATTACA AACAACAGAC ATTTATTCCT CATAGTCCTG GAGGCTGGGA AGTCTAAGAG 1560 CAAGGCACCA GCATATCCCG TGTCTGGTGA GGGCCCACTT CCTGGTTCAT AAATGGCACC 1620 TTCTCGCTGT GTCCTCGCAC GTGGAAGGGG CAAGGGATTT CTGTGGGGCC TCTTTTATAA 1680 GGACACTAAT CTCATTCATG AGGGCTCCCC CTTCATGACC TGATCACCTC CCAAATGCCT 1740 TCTCTCCTAA TGCCATCACC TTACAGATTA GAATTGCAAC ATAGGAATTT AGGGGGACGC 1800 AAACATTCAG TTCACTGCAG CAGCCAAAAG CAAAGTTACT ACCAAGAGAC CTCTGCCAGA 1860 CCCAGGGGAT TGATGAGACA TCTTGGTACA GGAAAGAGAA GGCATTCCTC ATCCAGGAGG 1920 ACGAGGACTG TGGCAGGACC CTCAGAGACC TGCAGGATGG CCCTAAGGGT GGTGGGAGAG 1980 GTGCACGGGT CTAATCCAGG ATTCATATAT AGATATATTC ATATCTATAT TCATATAGAT 2040 ATGAATATAT ATATATGAAT ATCTATACAT GAATATCTAT ATGAATATCT ATATATGAAT 2100 ATCTATATGA ATATCTATAT ATGAATATCT ATGAATATCT ATATATGAAT ATCTATATGA 2160 ATATACATGA ATATATGAAT ATATATGAAT ATATGAATAT CTATATGAAT ATATATGAAT 2220 ATCTATGAAT ATCTATATGA ATTATATATG AATATCTATA TGAATATATA TATGAATTAT 2280
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