| Tag | Content |
|---|
EnhancerAtlas ID | HS127-05642 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr11:61891640-61894070 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EGR1 | MA0162.3 | chr11:61891640-61891654 | TGCGCGTGGGCGTG | - | 6.2 | | EGR2 | MA0472.2 | chr11:61891642-61891653 | CGCGTGGGCGT | - | 6.14 | | EGR3 | MA0732.1 | chr11:61891640-61891655 | TGCGCGTGGGCGTGG | - | 6.25 | | Nr2f6(var.2) | MA0728.1 | chr11:61893888-61893903 | TGAACTCCTGACCTC | - | 6.22 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TGCGCGTGGG CGTGGGGATT GGGGGGTGGT TCGCGATTTT TTCCCCGGTC CTCTGCTCCG 60
TCCCTGTCGA CTCCGGACCA GGGTCGTGAC TCCCCACCCC AGCCCCTGGC TACCTGGGCA 120
TATGAGGGTC ACCTCTTCCA AGTGGCGAGG TCGCCTGCCT TGGTTCTCGG GCCCGAGATG 180
CCTCCCACCC TTTCCACCTA GGCCCTCAGC TTCCTAGAGC ATAGCCCCGT TCCCTCCGCT 240
CCCGGCTGCT TGGCACCTTG TGCCTGTGAG GATTAGTGTT GACTTGGACG CGCAGGAAGC 300
CCGAAACCAA CCCGGTTGTT TGGCGGAATG ATGCCAGATG GCATTTCTGT GCAGTTAAAC 360
CCCTCTCTCA ACGCCCCCGC CCCCAGCTGA GCAGCATTTT AAACTGACCA TTTCCGGAGG 420
CTGGGCCGCC CCTTGTCACT CCCCAAGCCT GTTCGCTGTC AGCGGTTCAG TCTCATTCAG 480
CTAACATGGG TTGCTCGCGG GGTTGCCCAG AGCCAAGACT GGGCACCTGC CTTTCAGAAG 540
TTGATATCTA GAAGGCGGTA TAGCCAGTGG TTAAGGGCAC GGTTTAAAGG CGGTATAGCC 600
CGTGGTTAAG GGCACGGTTC TATTTATGCC CCTGATTTAC CGGCTGATTT TGACTTCTCT 660
TTGCCTCAAT TTCCTCATCT GCCCATGCGT ATCCTCAAGG TTGTGGTGAG AATTAAATGA 720
GATGATGTCT GACTCGGGCA TGGAGTATGA CTCAGTAAAT GGGAGCAGCT GCTATGCGCT 780
TTCTGCACAG AGGTGTGGTA GGCGCCCAAC TTACAGCACC CTGAAAAGGA CAGGAGTCAT 840
AGAGGAGGAC GATGGGGCCT TCAGTCTGGT GTATGGTGTG GAAGAAGTGT TGGAGAGGAG 900
GAAGACTGGA GAGTGTCTTC CTCGGTGAGG TGTTGAGTGC TCTTTATCTG TGTGCAGGTG 960
CTTACATGGG TTGAAGAAGA GATTTTTGCT GCTCTTCCAG GAGCCTGATT CTTGGTACAC 1020
TGATTCCTTC TTTTTCAGGG TCACCTCTGT TTTAACTTAC GGTAACCCTT TTTAAATCGT 1080
TGCGCTAAGG TCTGCTAGAA GCAAACCTCC CCGTGAAAGA AGTCCAATTG CTTTCATGGA 1140
CTTTGTGAAA GAAGCTCTCA TCCACGTTGC CCATTTGAAC AAATACTTTT TAAAAAGTTA 1200
GCCAGTTGTT GCTTTTCTCT GCAAACCTTT GGCTTCCTTA AACAGTTTTC TCTTTTCTGG 1260
CCTGAGGTCC TGCGCTTTGC CAGGGCTGTG GTCTGGGTGC AGAAGGGTTA GGGGAAGGTG 1320
AGGGATGACA GTGAAAAGGG CTTGCCCATG ATTGGCTGGC TGCAGAGCCG AGGTTTCAGC 1380
CCAAAGCCTG TACGATCCTG CCCATTTGGC CCTGCCCTGA TTATTGCTGC CCTTGGCATC 1440
TGGGAACAGG GGTTTTGAAC ATGTGTTGGT CAGTTCTAAC CTGTGCAGAT TAAGTTTATT 1500
TGGTGCCCTT TGTGTGGTGG GATGAGCACC TATAGGATGT TTATTTCTAG GTGTAGAGTT 1560
GATGGGTGGA TTAATTCATT TAACAAATAG TCCTTGTTGC CAGGCACTGC TGTGCTCTGG 1620
GCATTCAACG ATGAGCAAGA CAGACAGGGG TTTGCCCTCA GAGAGCAATT GTTTAGTGGG 1680
CAGGGACAGG CAGTAAGCAA CAGGTAAACA AGCACGCAAG TGCTCTGCAG AGAATTACAA 1740
TCAATGAATG GGATCATGGC TGGGGCTACT TTAGATTGGT TTTCAGGTTT TCCTGAGGAT 1800
CTGAGATCCA AGCCATGAGG AGTGAGCCAT ACAAAATGTG AGACAATGTT CCAGACGCAG 1860
GGCAGAGCTT GTTGAGGAAC AAAGACTACT GTGTCCTTGA ATCAAGCCTG AGGAAGTCCC 1920
ATGAGACTGA AACCTGACCT GGTGCTACGC CCTGTGAGGG ATCAAGGGGT CAGCAATTTA 1980
TCCCTTCCTT ACAAGACCTT CCATTGTAGG TGGGAGGCTG AGTTGTGCAT GGTTTTTTTT 2040
TTTTTGAGAT AGAGTCTCCC TCTGTTGCCT GGGCTGGAGT GCAGTGGTGT GATCTTGGCT 2100
CATTGCAGCC TCTGCCTCCT AGGTTCAAGC GATTCTCCTG CGTCAGCCTC CTGAGTAGCT 2160
GGGATTATAG GCGTGCACCA CCACACACAG CTAATTTTTT TGTATCTTTA GTAGAGACTG 2220
GGTTTCACCA CGTTGGCCAG GCTGGTCTTG AACTCCTGAC CTCGTGATCT GCCCACTTCG 2280
GCCTTCTAAA GTGCTGGGAT TACAGGCGTG AGCCACCGTG CCCGGCCAGT TCTTGGTTTT 2340
AAAGAGGTAA GTCAGGATGG TGGATCACTG CCATTGACTT GAGGCATGCA GTTTGTTGTT 2400
ATGGCTTATG ACCACCACCC ATTCATTTGT 2430
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