Tag | Content |
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EnhancerAtlas ID | HS127-10042 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr14:92958580-92959810 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr14:92959237-92959255 | GGAAGGAAAGATAGAAGG | + | 6.46 | RREB1 | MA0073.1 | chr14:92959296-92959316 | ACCCCAAACACACACACACA | + | 6.95 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_09263 | chr14:92951570-92963512 | CD14 | SE_53529 | chr14:92957705-92959352 | Spleen |
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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 |
GH14I092491 | chr14 | 92957743 | 92959144 |
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Enhancer Sequence | CACCGTGAGT CTTTACAATT CCAAAACAGA TGCCTCATGC ATACTTGATT TCATCTGATT 60 CCGCCTCGTC ACTTACGTGA CTCTGTACAC CCCTGTCACT TCCCTTGGTA GTGAAGGATA 120 AAGGCAAGAA AATGTAGACG TTCATAGACA CACCCAAGTC CAGTCTTTGC CAAGAGCATT 180 GGCACTCTCG CTGTGCTTTT GCTGAGTACA TAAGAAGTCC CCAGAGGAAG CGAATTGCAT 240 TTCCTTTCTT GCTGCCTGGT CCAGTTCCTC TCTAGTGCCA GTAGGAGAGA GATCCTCCCC 300 TGCGCATCTG AGCTGACAAA TGGGAGGCAT GACATCCCTC AGGATGGCAC GTCGGAATAA 360 TTGAGGCCTC CCTACCCTAC ATGTCCAGGT CTGTGCTGAG CACTTGACTT CAGCGTCACT 420 TTATTCTATC CTTACAACCA CCTGATGAGG GAGGTGCTAT CATTCCCATT GCAGAAGAAA 480 TCGGGGCTCA GGGGTTAACT TTCCCAAGGT CACAGAATTG GGCAATGGCA AAGCTAGGAT 540 TTGAACCCAG GTTGGTCTGT CCTTAGGGAA CTCTGACTTT TTACTCGCAG TGCTCCAGTG 600 AGGTTCCTGG GATCCAGCCC CAGGAAGCCT TGATCGAGGG ACAAGGAGGA AGGCAGTGGA 660 AGGAAAGATA GAAGGATCAG GGAGGAATGT AAGATAATTC CGTGCTTTAA CCCTCTACCC 720 CAAACACACA CACACACACA CACACACACA CACACACACA CACACACACA CACACACACA 780 CAGAGAAAGA TTTGCCCAGC CAGGGGTCCA TAGGAGCCTT GGAAATTGTG CTAAGGAGAC 840 AAGGGAAAAG ACCATGGTTC CACGCTCTGA AGCACAGGGG TCATCCAGCT AAAGCCCCCA 900 TTTGTCTCTA GAGAAGGCCT GGGCAAGGAG GACCACATGC CTACGACCAG CCGGGAGGAA 960 GTGACGTGCC TGCCTGGGGA GGGCCGGTCC CATGAGGGCG GCTGCTGTGT ATCCCTGAGT 1020 CAATGCGGCT AGGACAGAGA CTCGCCCTTT CATGGGGCAA GTCTAAGCCC TCTAGGGCTT 1080 ATTCTGGTCA AACTGAGGAT CAGACTGCAG CACCCCGCTA CACTTGCCCA CATTCTGCAG 1140 AATGTTCTAG GTTTCCCCAC ATAGGTGTCG CTTTCCAGTA GAAATGCCTC TTGTATTTCT 1200 TTGCCCTGCA AGCCCAGTTC CCACACTCTG 1230
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