Tag | Content |
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EnhancerAtlas ID | HS092-10598 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr11:118562370-118564130 |
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: 3 | Chromosome | Start | End |
chr11 | 118562675 | 118563898 | chr11 | 118562658 | 118562793 | chr11 | 118562463 | 118563803 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I118691 | chr11 | 118562342 | 118564020 |
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Enhancer Sequence | CCTGAGTCCA GGAGACAGGA CAGGGTCACT CATCTCTGTC CCTGGTGATG GAAACTCAGG 60 CTCAGGAAAG AGCCTTGACC TGCCCTGGGT CACAGAGAGA ATATTAGGGT CAGGGCTTGA 120 GCCCGGGTGC TGTGGTCAGG CCCTTAGGCC GCCTCTCACA CCCAGACTAG GAAGCTGGAG 180 CAGAAAGTTT GCTAGAACAA TCCTGAGAAG AGGCCTGCAC AGTTCAAGGG GCAGCTTGGA 240 GGAGGAGAGG GAGGGAGGAC CGGCTCTGGC CAGTGGGCTC TTGGACCTCA GGCCAGGCTC 300 TGGCAGCTGC ATCTGGTATC AGGCCTGCAG GTCCAGTGCC TATTATGGGG CCTATTATGA 360 CTGCACAAGG GGCCTCAAGT TCATTCAGGC CAAGCCTCTC ATTCTGCAGA GAACCACACA 420 GTGGTTGCCG GGATTTGCCC AAGGCTGGTG GGTTGGTCAT GAGGGCAGGC CCGAACTCAT 480 CTCTATTTTC TTGCATTCCG GCTCTCCTGA TGTTCCAGGC CCATCTCTGA GTCATCCTTG 540 GACAGGAGAG ATCCCAGAGG GTAAACAGGA CATGAGCCTG CAGTGAGGGG AGACAGAGGA 600 GGAGAGAACT CCCTGAAACA AGAGGAGAGG AGGAGCTGGT GGGGAGGACA CAGGTAGGGC 660 AGCGGGCAGA CCACCAAGGG GCAGGCTTGC TGTTTCGCAG CCTGACCCCC AGCCTGTGTG 720 CCTCATTGCC GCCTCCTCCT CCCAGAGCAG GGCCTACGCC TCAACCAGAG CTTGGAGCAA 780 GACAAGGAAG GCTCCATTTC TCTCCTCCTA CTCCTCTACT CAAACCACAG CCATCTGTAC 840 ATCAGAAACT TTTTTTTTTT TTTTTTTAGC CCTCAGCTGC CTGATGCCCA TGGTTGGGGT 900 TTGGGCTGAG TCACCGAGGG CTGCCTGCAC ACACCAGGGA GGGCTCCTGA GCACCCACTC 960 TCAGGCTTTG CACGTTTCCG AAATTCTGCA CACGACAGCA ATTTTTGCAG CAAGGGTGTG 1020 GAGGGTGCCT GTGGGCCAGT CACCAGCCTG CTGCAGCTGT CCGTGGTTGC CTCTGTCTGC 1080 CAGGGCTGCA CGACCTCTGG TTTTCACCTC AACCACTGCG GCTTCCTCTC TCCCCGTGGG 1140 AACAGGGCAT GGGGTGAGGG AGCTACCATG CCCAGACAAC TAGGCATCTC CCTGCCAGGC 1200 CAGGAGTTCC ACTGCCACAG CCCAATACCA GCAAATTCAG ATGCAACCAA GTGACCCCAA 1260 CTCAAGTTAC ATTCCCTTTC TCCCCCACAG GCTCTGCAGT CCCAGGGATT CGCAGTGTTA 1320 GTTGATCTCC GGGGACACTA GTTCCCAAGA GACCCCACTG AAGGCCTGGC TGTACCATCA 1380 TAGGCTGTGT GCCCTTGGGC AAGAACCTCT ACCATTCCTC GTTGCCTGTA TATAAATTGA 1440 AGGCTTTGCT CTAGGTCAGT GTTGCAAACT CAAATTCCAG TAATAGGAAT GTGCAAAATA 1500 TGTTGGGGAT AAGGGAGCCA ACAGTGCAAG GGGGAAGTGA GTGTTGGGGA CCTAGTCTTG 1560 GGGTGACGGG AACTGGGCTG AACCGGAAGC GTATTCCTGT GTAAGGGAGG CCACTGCTCA 1620 GAGGGTGGCT GCTATGGGGC TGGGGGATCC TGATTTGTCA AAGGAAGGTG GAAATTTATA 1680 TTTCAGCTCA CACGCTCCTG TTTTTAAAAT GTCTCAATGT CTCTAATTCT GACTGTAAAT 1740 CTAAGAGTGA TTCCTGTGTG 1760
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