Tag | Content |
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EnhancerAtlas ID | HS127-07238 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr12:47710340-47711710 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CDX2 | MA0465.1 | chr12:47710904-47710915 | TTTTATTGCTT | - | 6.32 | Foxd3 | MA0041.1 | chr12:47711066-47711078 | GTTTGTTTGTTT | + | 6.32 | SPI1 | MA0080.4 | chr12:47711047-47711061 | AAAAAAAGGAAGTT | + | 6.11 | ZNF263 | MA0528.1 | chr12:47711150-47711171 | CTCACTGCCACCTCCTCCTCC | - | 6.11 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 47711000 | 47711452 | chr12 | 47710400 | 47711000 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I047316 | chr12 | 47710218 | 47711583 |
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Enhancer Sequence | AATAATTCTA TAAGAAAGAA TGGAGATACA ATATTTGATC TAGAAAGTGG ATATCCAATG 60 ATCATCTGAG CAAGGAACAC CATCCTCCTT AAAGTAAACA GCACACAGCT GTTTCCATCA 120 TGCTGACTGT AAGAAGATTA TCATACTCAG AAAAGAAATT CCAGGAAACT GCGTTCCAAT 180 TAACATGGAA ATGAATCCAC AAAATAAATA TGTATCCAGA GTTTATGCAA TCCCAGGGTA 240 CAATGGAGAC AGATGCAGAT TGATCTAATC TGGTTGCATT AGGAATAAGA ATGTTTGTTG 300 GGGAACATTG TGTGGAAAGT TGACATTTGG TTCAATCAGG AAGGCCAAAG TAGAAATTAT 360 GAAAGCAATT TCCTTTGTCC AGTTAAATTA GGCATTCAAA TAACAGGCTA CTCTTTGACC 420 TTCCTGGGAA AGGTCAGGAT GGCATCGAAT GGTCATTAAA TAAATAGCAG GCCTGTTCTT 480 GTAAATACTT TGTGAGACTT TAGGAAAACA TATTCTGGAT TGAAAATCAG CCAAAAAAGA 540 TCTGCAAGAA TTTCTCTAAC ATATTTTTAT TGCTTCTATT TATCCATTTT TAATTTGGAG 600 AAATAGTAAG TACTGGTAAA AGCACAAGAA CAAACTGAAT ATGGGGTCTA TTGAACAAAA 660 TTAAGAGGTC ACTTTTCTGC CACTTGCTAA TATGTGCTGC AGCTGCTAAA AAAAGGAAGT 720 TTTGTTGTTT GTTTGTTTTG GTTTTGGTTT TGGTTTTGAG ACGGAGTTTC GCTCTTTTGC 780 CCAGGCTGGA GTGCAATGGC GTGATCTCGC CTCACTGCCA CCTCCTCCTC CCGGGTTCAA 840 TTGATTCTCC TGCCTCAGCC TCCCAAGTGG CTGGGATTAT TGGCAGGTGC CACCATGCCT 900 GGCTAATTTT TGTATTTTTA GTACAGACGG GGTTTCACCA CGTTGGCCAG GCTGGTCTTG 960 AACTCCTGTC CTCAGGTGAC CTGCCCGCCT TGGCCTCCCG AAGTGCTGGG ATTACAGGCG 1020 TGAGCCACCG CACCCAGCCA GAAAGAAGGT TTTTTGAAAA ATAGCTCCTG TGGATGTCTC 1080 CCCAAGGCTC CACTTGATAT AGCTAAGGAG AATTCCTGGC ATGTATCATA AGATATATGG 1140 TTTCTTAATT AGATGGGTGA CTTGCAGGAC TAGAATTTAA GAACACTCTT CATGCTGCCT 1200 TAGGTTATAA TTCCCAGCTT GCATTACAGC AATGGACATG CTGTTAATAT TTTCTCCAAC 1260 AGTCCAAACT GCAAGTATAT GAAGTTAAAT CAAATCTCTT TTCTTGTCCA TTAAAGTTCA 1320 AGTTGCCATA ATAAAAGCTG GCAAGTTGTT TTTATAAACA CTAAATTAAT 1370
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