Tag | Content |
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EnhancerAtlas ID | HS127-08359 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr12:133360890-133362100 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr12:133361290-133361310 | CCACACACCACACACACACG | + | 6.35 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 133361419 | 133361525 | chr12 | 133361803 | 133361857 |
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Enhancer Sequence | TTCCTAAGGG CCAAGATGGA ACGGGCGCTT GGTCATGGGA CAGGCCCTGA CCCCCCTCAC 60 TTCCTGTGGT GCCGGCAGGC ATGAGGCTGT GTGGCTGCAC ACACCAGACA CCAGCTGTCT 120 GACACAGTCT CACAACCTTC CTTTTTGTTA AAGAAGTTGA ATTAACCGAC CACAGCATGC 180 ACACGATGAC ACACGGGGAT AGTTGGGACA AACAAAATCA TCTCTTCAGT TCAATGCTTC 240 AAAAATACAG AAGAAAATCT GACCTGCAGA TAATGGCTAT AAATCACCAT CTGTGGCAAG 300 CAAGCAGCAC CAGTTGTAAT AAATACCACA CACATGCTCA CGCACCACAC ATCACATACA 360 CACACTCATG TAACACACAC CACGTGCACA TGTTCACATC CCACACACCA CACACACACG 420 TGCTCACACC CCACACGCAC ATGCTCACAC CCCACGTGTT CACACCCCAC ACCACACATG 480 CACATGTGCT CACACCTCAC ACTGCATGCA CACATACACC CCACACTGCA TGCACACATA 540 TGCTCACATC CCACACACCA TGCACACAAA CACTCCACAC GCTGCACACA CACATGCTCA 600 CACCTCACAC ATGCACGGAT ACATGCAGGC ACAGGTGTGC TCTCACACCC CGCCCACTTG 660 CTGCCTCGAT GGTACCAGGC CCTTGCCAAG CATGTTCCAG TACCACCTAA CTTAACCCTT 720 ACATGAGAAG GTTCTCATTC ACCTCAATTT GGCCTCATTT TGCTGAGGAT CAAAAAGGTG 780 AGAAATTTGC CAAAAGTCAC CACTTGCGAG GGGTGAAGCC CGGACGGACA CAAGACATCG 840 GCTCGCAGCT GTGCTATTCC TCAGCTGCAA CAGCGTGGCG AGGGGCCAGC TCTGCCCGGC 900 CTTTGCGACC TCCCCACCCC AGCCCTTAGT GAGCCCAAAG AAAATGGCAA CTGAATCAAT 960 CTCCCCAACA TTTTACAAAG CAACCAGGTG AGAGGAAGCA CTTGATTTAT TTATTGAATT 1020 TCAGACACAG AGTCTCTATC GCCCGGGCTG GAGTGCAGCA GCAAAATCAT GACTCACTGC 1080 AGTTTCAGCC TCACCTCCCA GGCTGAGGCG ATCCTCCCAC CTCAGTGTCT CAAGCATCTG 1140 TGTCCACAGG CACGTGCTAC CATGCCTGGG TTTTATTTTT GTATTATTTG TAAATACAGG 1200 GTCTAATTAT 1210
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