Tag | Content |
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EnhancerAtlas ID | HS098-11476 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr11:118562470-118564000 |
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: 2 | Chromosome | Start | End |
chr11 | 118562675 | 118563898 | chr11 | 118562658 | 118562793 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I118691 | chr11 | 118562342 | 118564020 |
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Enhancer Sequence | ATATTAGGGT CAGGGCTTGA GCCCGGGTGC TGTGGTCAGG CCCTTAGGCC GCCTCTCACA 60 CCCAGACTAG GAAGCTGGAG CAGAAAGTTT GCTAGAACAA TCCTGAGAAG AGGCCTGCAC 120 AGTTCAAGGG GCAGCTTGGA GGAGGAGAGG GAGGGAGGAC CGGCTCTGGC CAGTGGGCTC 180 TTGGACCTCA GGCCAGGCTC TGGCAGCTGC ATCTGGTATC AGGCCTGCAG GTCCAGTGCC 240 TATTATGGGG CCTATTATGA CTGCACAAGG GGCCTCAAGT TCATTCAGGC CAAGCCTCTC 300 ATTCTGCAGA GAACCACACA GTGGTTGCCG GGATTTGCCC AAGGCTGGTG GGTTGGTCAT 360 GAGGGCAGGC CCGAACTCAT CTCTATTTTC TTGCATTCCG GCTCTCCTGA TGTTCCAGGC 420 CCATCTCTGA GTCATCCTTG GACAGGAGAG ATCCCAGAGG GTAAACAGGA CATGAGCCTG 480 CAGTGAGGGG AGACAGAGGA GGAGAGAACT CCCTGAAACA AGAGGAGAGG AGGAGCTGGT 540 GGGGAGGACA CAGGTAGGGC AGCGGGCAGA CCACCAAGGG GCAGGCTTGC TGTTTCGCAG 600 CCTGACCCCC AGCCTGTGTG CCTCATTGCC GCCTCCTCCT CCCAGAGCAG GGCCTACGCC 660 TCAACCAGAG CTTGGAGCAA GACAAGGAAG GCTCCATTTC TCTCCTCCTA CTCCTCTACT 720 CAAACCACAG CCATCTGTAC ATCAGAAACT TTTTTTTTTT TTTTTTTAGC CCTCAGCTGC 780 CTGATGCCCA TGGTTGGGGT TTGGGCTGAG TCACCGAGGG CTGCCTGCAC ACACCAGGGA 840 GGGCTCCTGA GCACCCACTC TCAGGCTTTG CACGTTTCCG AAATTCTGCA CACGACAGCA 900 ATTTTTGCAG CAAGGGTGTG GAGGGTGCCT GTGGGCCAGT CACCAGCCTG CTGCAGCTGT 960 CCGTGGTTGC CTCTGTCTGC CAGGGCTGCA CGACCTCTGG TTTTCACCTC AACCACTGCG 1020 GCTTCCTCTC TCCCCGTGGG AACAGGGCAT GGGGTGAGGG AGCTACCATG CCCAGACAAC 1080 TAGGCATCTC CCTGCCAGGC CAGGAGTTCC ACTGCCACAG CCCAATACCA GCAAATTCAG 1140 ATGCAACCAA GTGACCCCAA CTCAAGTTAC ATTCCCTTTC TCCCCCACAG GCTCTGCAGT 1200 CCCAGGGATT CGCAGTGTTA GTTGATCTCC GGGGACACTA GTTCCCAAGA GACCCCACTG 1260 AAGGCCTGGC TGTACCATCA TAGGCTGTGT GCCCTTGGGC AAGAACCTCT ACCATTCCTC 1320 GTTGCCTGTA TATAAATTGA AGGCTTTGCT CTAGGTCAGT GTTGCAAACT CAAATTCCAG 1380 TAATAGGAAT GTGCAAAATA TGTTGGGGAT AAGGGAGCCA ACAGTGCAAG GGGGAAGTGA 1440 GTGTTGGGGA CCTAGTCTTG GGGTGACGGG AACTGGGCTG AACCGGAAGC GTATTCCTGT 1500 GTAAGGGAGG CCACTGCTCA GAGGGTGGCT 1530
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