Tag | Content |
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EnhancerAtlas ID | HS136-06381 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr14:103827960-103829110 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr14:103828409-103828422 | TTCTGGAATTTTC | + | 6.17 | NFAT5 | MA0606.1 | chr14:103828416-103828426 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr14:103828416-103828426 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr14:103828416-103828426 | ATTTTCCATT | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr14 | 103828242 | 103828602 | chr14 | 103828081 | 103828691 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I103361 | chr14 | 103827555 | 103829319 |
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Enhancer Sequence | TGTATACCTA CATACCCATG ATAAAGTTTA ATTTATAAAT TAGGCACAGT AAGAGATTAA 60 CAACAATAAC TAACAATGAA ATAGAACAAT TATAATAACC TACTGTAATA AAAGTTAAGT 120 GAATGTGGTC TATCTCTCTC TCAAAATATC TTATTATACT TTATTCACCC TTCGTATGAT 180 CATGTGAGAT GATAAAATGC CAGCATCACT ACTCGTGCCC TTTGGGGCCA TTATCAATGA 240 AAACAGGAGT ACTTGAACAC AAGCACTGTG ACACCGTGAG AGCCGATCAG AGATGGCTGC 300 TGAGTGACTA ATGGGGCAGG TAGCATAGAA AATGTGGATA CGCTGGACAA AGGGATGATT 360 CACATCCTAA GCAGGATGGA GCAAGCTAGC AAGAGATTGC ATCATGCTCC TCAGAATGGT 420 GCACAGTTTA AAACTTATGA ATTGTTTACT TCTGGAATTT TCCATTTCAT ATTTTTGGGC 480 CACAGTTGAC CATGAGTAAC TGCAACCACA GAAAATAAAG CCTTGGGTAA GGAGGGGCTG 540 CCGTATCATA CTCTGCCCCT ATACGGCTCT GCCACCACCC TCTCAGCTAA TGATGTCAGA 600 AGTTATACCT TTATACATTG GGTGCCAAAA AACATAGACT TATTACTGGC TTTTTACTAT 660 TAGTCTTTTA AATCATGTAT AAAAGGAAAA GTGGTGTTAC AACCCAAAAT GACAATAATA 720 CTAGCTTTTG TAATTGTCCA TGTATTTACC TTTATAGAAG ATCTTTATTT CTTCATAGGA 780 CTTTGAGTTA TTGTCTAGTG TTCTTTAGTT TATTTTTTTT TAATTTTTGC TTTCTTCCTT 840 CTGCCTATAT AATGGCAAAT ATCCTTTAAT TTCAATCTGC AGAAGTCCCT TTAGCATTTT 900 CTGTAAGACA GATCTAGTGG TAATAAACTC TTTCTGCTTT TGTTTATCTG GGAATACCTT 960 CATTTCTTCT TTTCTGAGGG CAGTTTTGCC AGGTATAGGA TTACTTTTGT TTTGTTTTGT 1020 CTTCTTTTTT AAGAGACAGA GTCTCACTCT GTCAGCCAGG ATGGAGTGTA GTGGTGTGAC 1080 CATAGCTCAC TGCATCCTCA AACTCCTTAG CTCAAGTGAT CATCCCTGCC TCAGCCTCCT 1140 AAGAAGCTGC 1150
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