Tag | Content |
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EnhancerAtlas ID | HS127-07256 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr12:48689930-48690970 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MAFK | MA0496.2 | chr12:48690418-48690437 | AATGACTGAGTCAGCATTT | + | 6.28 | Mafb | MA0117.2 | chr12:48690426-48690438 | AGTCAGCATTTT | - | 7.22 |
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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 |
GH12I048296 | chr12 | 48689901 | 48691424 |
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Enhancer Sequence | GTGCCAGGAC CACAGATCCT TTGACTCACA CCATATATTC TGCCTCCCAA GTCCTTATCC 60 CACGGTGGGC AATCATTTTC CTCTCAAAGC CCTTTATCAT ATTAAATTCA ACAAACATCA 120 TATACCTCCT GGCTATTTTG CGCCGAGCAC TGTTCTGGGC ACCTTTACAT ATTTGGGCTT 180 TCCAGTTTGC ACTCTCAAGG AAACAAACAA AAAGAAAGAA AAACCTGACA CGACCCCCTT 240 CACCCCTCGC CCCACCCACT TTCCCACCTA CACACCCAAA ATGCTTAGGT GAGCAGAATG 300 AAAGGCTGAG CTAGATTCTG GAACACTTTT AAGGAAAGAG ACGGAAGGAC AGTAGGGTCA 360 GTTCTTCAGG AGGGTGAAAA TTAGGAGGCT ACCAAATTCT ACCCCAGATT ATCTATAGTC 420 TCCCACCCAT TTTTCATTCG TTTATGCCTC AGTAATAAGA AGCACGACAG TCTTTTCCCT 480 CAGCAGTCAA TGACTGAGTC AGCATTTTGA GGCAGCGCCG CCTCTCAGGC TCCAGGACAC 540 AGGACGCCTT GAGACTACAT TTCCCACAGG CCACAGCCCA GCCTCCCGTC TTCTAACAGT 600 CTTCCTAGAA AGGTGCGCAT GTTCCGACCA TTAGCACACG GCTGGTGCGC TCGGTGCAGG 660 CTATCGGAGC CCGGGACAGG GCCGATCCAG CCAGGCTTCA GGGTGCGGGA AACGGGTGCG 720 CCATGAGATA GAAGCTTTCT GCTTCCACCC ACTCCAGGCG CCCAGTCTTT CTCCAGCACC 780 TCTTAAGCTA GCCCCAGGAC TCTGCAAGGT ACCCGAGGAC AGGAGTCACT GCTTGCATCC 840 CCTCAGCCTT GGGGCAAGAA GAAGGAGCCA GAATCCAGGA AAGGGGCTTT GGCGAAACTG 900 CACGGAAATC ATTCCTTCCG TTTACGTAAT TTTAGTTTTA AGTGTAGCAG CCGGGGAGAA 960 AATTGTGAAG GGGAGTGAGA CAAGCGTTCG ATTACTTAGC CAATTGTAGT GCACAACTGA 1020 AGTTGCAGAC CTGAAGAAGC 1040
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