Tag | Content |
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EnhancerAtlas ID | HS095-24665 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr5:132575760-132576910 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
JUN(var.2) | MA0489.1 | chr5:132576362-132576376 | ATGACTCATCTCTT | - | 7.19 | JUN(var.2) | MA0489.1 | chr5:132576381-132576395 | ATGACTCATCTCTT | - | 7.19 |
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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 |
GH05I133240 | chr5 | 132575801 | 132577835 |
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Enhancer Sequence | AGGTTTACAC TGACTTTATC AGCTGCAACA CTCACCCTGA AGGTCTGCAG CTGCACTTCT 60 GAAGCCAGCG AGACCACGAA CCCACCAGAA GGAAGAAACT CCAAACGCAT CCGAGCATCA 120 GAAGGAACAA ACTCTGGACA CGCTGCCTTT AAGAACTGTG ACACTCACTG CGAGGGTCCG 180 CGGCTTCATT CTTGAAGTCA GTGAGACCAA GAACCCACCA ATTCCGGACA TAATAGACGG 240 ACTTGCCATC CTGCAAAGAC CTGAGGAACC ATCCTTTTTC TCAGAGTCCT CTCAAGAAAA 300 AGAAGTCTCT GCAACTTGGA GCAATCTCTA AGTAGCTGTC TGAGCCCCCT GGAAGAGGGC 360 TGTTGTGGGC AGCTGCATTC AGTGTGAGCA ACCTGGAGTG GGCCTGTCCT CCTGCTCGTT 420 CCCAGGTTCA GGCCTGGAAG AGGGAGTTGG AGGCATGAGA GAAGCCACTG TGGGGAGAGC 480 ACCTGGTTCT TCCAAGGCTC GGGGCATGTG TGGTCCCTGG CTGACTTGGG TGTCCTCTGG 540 TGTGTGCGGT CAGTCTTCTT CTGACTGTGG ATGCCAAAGG GGAGGCCCTT ATCTCTTAGC 600 GCATGACTCA TCTCTTCGCG CATGACTCAT CTCTTTGTGC ATGACTGTAT TATTCTCAGC 660 GTGTCATGTG GTTCCTGTGC ATAACTGAGC TCAATGAATA TTTGCTGATT TCAGGGAGTG 720 TGTTAGCCTA GGATGCTACC TCCTGGGAAG CCCTGAGAGG AAGGATAGTT AAGAATTCAT 780 ATTACCCAGG GAGGTCTGGC CTTGCCCTCT TTGGCTACAG GGAGGCAATC TCTAGGCTCT 840 GGAATGTCAT GCCTCATAGG GGTCTCTTTA TTTGCCTGGG GTCTTTGGGC CAGGTGGTAC 900 CAGTTCTGTC TCTAGAGGGG CTGGGGACGA GAGGGCAGCC ATGTGGGCAG TATTTGAATG 960 AGCTCCAGCA AAAGCTTTGG ACACCGAGGC CTGGGTGAGC TTCTCTGGGA AATTGACACT 1020 GTGACAGTGA CATGTCTGTG ACTCCACTGG GAGAGGAGAA CAGAGATTCC ACGTTTAGAG 1080 CCCTCCTGGG CTCTGCCCTT TGGGCTTCAT CACTTGGCTG ACTTTAATCT GTACTCTTTT 1140 TGCTGTATTA 1150
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