Tag | Content |
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EnhancerAtlas ID | HS105-16311 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr11:118562450-118563780 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr11:118562896-118562907 | CTGAGTCATCC | - | 6.32 | JUNB | MA0490.1 | chr11:118562896-118562907 | CTGAGTCATCC | - | 6.14 | Myog | MA0500.1 | chr11:118563420-118563431 | CTGCAGCTGTC | - | 6.62 | Tcf12 | MA0521.1 | chr11:118563420-118563431 | CTGCAGCTGTC | - | 6.14 | ZNF263 | MA0528.1 | chr11:118563166-118563187 | TTTCTCTCCTCCTACTCCTCT | - | 6.37 | ZNF263 | MA0528.1 | chr11:118562607-118562628 | GGAGGAGGAGAGGGAGGGAGG | + | 9.66 |
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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 |
GH11I118691 | chr11 | 118562342 | 118564020 |
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Enhancer Sequence | TGCCCTGGGT CACAGAGAGA ATATTAGGGT CAGGGCTTGA GCCCGGGTGC TGTGGTCAGG 60 CCCTTAGGCC GCCTCTCACA CCCAGACTAG GAAGCTGGAG CAGAAAGTTT GCTAGAACAA 120 TCCTGAGAAG AGGCCTGCAC AGTTCAAGGG GCAGCTTGGA GGAGGAGAGG GAGGGAGGAC 180 CGGCTCTGGC CAGTGGGCTC TTGGACCTCA GGCCAGGCTC TGGCAGCTGC ATCTGGTATC 240 AGGCCTGCAG GTCCAGTGCC TATTATGGGG CCTATTATGA CTGCACAAGG GGCCTCAAGT 300 TCATTCAGGC CAAGCCTCTC ATTCTGCAGA GAACCACACA GTGGTTGCCG GGATTTGCCC 360 AAGGCTGGTG GGTTGGTCAT GAGGGCAGGC CCGAACTCAT CTCTATTTTC TTGCATTCCG 420 GCTCTCCTGA TGTTCCAGGC CCATCTCTGA GTCATCCTTG GACAGGAGAG ATCCCAGAGG 480 GTAAACAGGA CATGAGCCTG CAGTGAGGGG AGACAGAGGA GGAGAGAACT CCCTGAAACA 540 AGAGGAGAGG AGGAGCTGGT GGGGAGGACA CAGGTAGGGC AGCGGGCAGA CCACCAAGGG 600 GCAGGCTTGC TGTTTCGCAG CCTGACCCCC AGCCTGTGTG CCTCATTGCC GCCTCCTCCT 660 CCCAGAGCAG GGCCTACGCC TCAACCAGAG CTTGGAGCAA GACAAGGAAG GCTCCATTTC 720 TCTCCTCCTA CTCCTCTACT CAAACCACAG CCATCTGTAC ATCAGAAACT TTTTTTTTTT 780 TTTTTTTAGC CCTCAGCTGC CTGATGCCCA TGGTTGGGGT TTGGGCTGAG TCACCGAGGG 840 CTGCCTGCAC ACACCAGGGA GGGCTCCTGA GCACCCACTC TCAGGCTTTG CACGTTTCCG 900 AAATTCTGCA CACGACAGCA ATTTTTGCAG CAAGGGTGTG GAGGGTGCCT GTGGGCCAGT 960 CACCAGCCTG CTGCAGCTGT CCGTGGTTGC CTCTGTCTGC CAGGGCTGCA CGACCTCTGG 1020 TTTTCACCTC AACCACTGCG GCTTCCTCTC TCCCCGTGGG AACAGGGCAT GGGGTGAGGG 1080 AGCTACCATG CCCAGACAAC TAGGCATCTC CCTGCCAGGC CAGGAGTTCC ACTGCCACAG 1140 CCCAATACCA GCAAATTCAG ATGCAACCAA GTGACCCCAA CTCAAGTTAC ATTCCCTTTC 1200 TCCCCCACAG GCTCTGCAGT CCCAGGGATT CGCAGTGTTA GTTGATCTCC GGGGACACTA 1260 GTTCCCAAGA GACCCCACTG AAGGCCTGGC TGTACCATCA TAGGCTGTGT GCCCTTGGGC 1320 AAGAACCTCT 1330
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