Tag | Content |
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EnhancerAtlas ID | HS047-09170 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr13:31263680-31265570 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP2 | MA0593.1 | chr13:31265044-31265055 | AAGTAAACAAA | + | 6.62 | IRF1 | MA0050.2 | chr13:31264420-31264441 | ACAGCGAAACTGAAAGAGCAC | - | 6.16 | KLF14 | MA0740.1 | chr13:31264023-31264037 | TGCCACGCCCCCAT | + | 6.72 | KLF16 | MA0741.1 | chr13:31264024-31264035 | GCCACGCCCCC | + | 6.62 | Klf1 | MA0493.1 | chr13:31264564-31264575 | AGCCACACCCT | + | 6.02 | SP3 | MA0746.2 | chr13:31264023-31264036 | TGCCACGCCCCCA | + | 6.41 | SP8 | MA0747.1 | chr13:31264024-31264036 | GCCACGCCCCCA | + | 6.11 |
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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 |
GH13I030689 | chr13 | 31263676 | 31265628 |
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Enhancer Sequence | GTTCTGAGAT TCTTCTCCAT TACTCTGACA GGTTGGACCC TCTGGGGAGC AGATCTCAAG 60 ATCAAGTTAT GAGTGCAAGA GGTGTGTTGG GAAGCGATGG TTGTAAAAGA ATCCTGCAGT 120 AGCACCAGGC ACAAGTCTGT CCAGGGAGAG GAGGACTTCT ACTCTCTACC AGCATCTCTC 180 CTAAGTCCCC TTAGGGGACG GGGGCAAGGA AGTGCTGGGA AGGGCAGGGC ATGGTTCCTG 240 GCTAGGACTC CACCCCCCTG GGGCCTGTAC CCACGGACCT AGGTGAAGAC AGGCACTCCT 300 GCCTTCTCGC CCAACGGTTG CGTTTCCCAA GATCATCCTG GCCTGCCACG CCCCCATCTA 360 CCTATTAAAC TCCCCCACCT TCCCCAAACC CTAGCAGGCA GACACACATC GGTGGAAGAA 420 GACAGGAGCG GCTGGACATT GAAAGGACGT CGAGAGGAGC ACACCTGCAC ACCATCGACC 480 AGCGGAACGA GGCAGAGTGT GGCTGGAGCA GTCGGAGGGA AGCCTGGGCC GCTGACTCCA 540 GGGGAAAACC ATCTCCTTTC TGGCTCCCCC CTCTGCTGGG AGATACTTTC ACTGAATAAA 600 ACCTTGCACT CATTCTCCAA GCCCACCTGT GATCCGATTC TTCCTGTACA CCAAGGCAAG 660 AACCTGGGAT ACAGAAAGCC CTCTGTCCTT GTGATAAGGT AGAGGGTCTA ACTGAGCTGG 720 TTAACACAAG CTGCCTATAG ACAGCGAAAC TGAAAGAGCA CACAATAGCA CACACTCATT 780 GGGGCTTCAG GAGCTGTAAA TATCCACCCC TAGACGCTGC CATGGGGCGG GAGCCCCACA 840 GCCTGCCCGT CTAGAGGTTT GAGCAGCGGG ACACTGAAGA AGAGAGCCAC ACCCTCATCG 900 CACGTCCTGC GAGGGAGACA AGGGAACTTT TCCGGTTTCA CTTCTGCTTG GCTTGAGCTG 960 GCACTGAAGC ACCCTTTTCC CTCCTCACTG AGGGAGCAGA GGGGAAAAGC GGTAGAACTA 1020 ACAGGCTAAC AATGCTCCTC CGAAAATATA TCGTATTTTT GGATCCCTAG AGATAGGTGA 1080 TCACGGCAGC CGCGGAGTGC ATTTGGGTCT CCTTTCAAGA AAGAACTTGC TGCTCAGCGT 1140 TGAAGAATGC AGTTGGCCAA CAGCCTCCAG CTGCTCTGTC TTCAGCATCT GCCATGGCAT 1200 CTGAGCTGAG GTCATGTTCT TCCTGGGAGG TCCCCAGCAG AAGGATCACG TGGAAGCTCC 1260 ACAAGCTCCA CAGATGTTCC AGGAGAGGAA TAGGCAGCAT TTGGAAGACA TATCCTGCCA 1320 TAACAGAGGG CATTTGCTAG TAGAGACAAC AAACAGCAAC AGCCAAGTAA ACAAACACAC 1380 AAGCACAAAG CACTTTCTCC CATTTCCCCT CATTGATCCT GTCCGGGTAG AAGCTGGGGA 1440 GGAAGTAGAA TAGGGTGAGG CGGGGTGGGG CTGGGGGGCC TACACCTTCT TCCTTCCCCC 1500 GCAGGTCCTG TCCCTGGGCC AGGCTTGAAC TAGGGGAATG GGAAAAGCTG TGAAGTGAAT 1560 GAGAATTAGG AGTTTTTATT TAGACTGGAC TTGAATTTTT TTTTTTTTTT TTTTTTTTTT 1620 GAGACAGAGC CTCGCTCTGT CACCCAGGCT GGAGTCCCGT GGCGCCATCT TGGCTCACTA 1680 CAGCCTCTGC CTCCCGGGTT CAAGCGATCC TCCCACCACA GTCTCCTGAG TAGCCGGGAT 1740 TACAGGTGCC TGCCACCATG CCCAGCTATT TTTTTTTTTT TTTGTATTTT TAGTAGAGAC 1800 AGGGCGTCAC CGTGTTGGCC AGGCTGGTCT CGAACTCCTG GCCTCAAGTG ATCTGTCCGC 1860 CTCGGCCTCC CCAAGTGCTA GGATTATAGG 1890
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