Tag | Content |
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EnhancerAtlas ID | HS098-12098 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr12:1946770-1948030 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RFX1 | MA0509.2 | chr12:1947806-1947822 | TGTTTCTATGGCAACC | - | 6.31 | RFX1 | MA0509.2 | chr12:1947806-1947822 | TGTTTCTATGGCAACC | + | 6.32 | RFX2 | MA0600.2 | chr12:1947806-1947822 | TGTTTCTATGGCAACC | + | 6.73 | RFX2 | MA0600.2 | chr12:1947806-1947822 | TGTTTCTATGGCAACC | - | 6.8 | RFX5 | MA0510.2 | chr12:1947806-1947822 | TGTTTCTATGGCAACC | - | 6.79 | RFX5 | MA0510.2 | chr12:1947806-1947822 | TGTTTCTATGGCAACC | + | 6.87 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_33402 | chr12:1927823-1955818 | H2171 |
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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 |
GH12I001838 | chr12 | 1947101 | 1947250 |
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Enhancer Sequence | TTTGGATAAC AACCCAGCGA GCCAGGAGCA AACCCTAGAG GGAAGTGAAC CATCAGGGTC 60 CCCCGGGAGT TCAGCTCCAT TCCATGGCAG AGCTGGGGTG TCCGCCTTCC CCAGGTGGTG 120 ATAAGTGTAG GGATGTTGCT CTCCTATAGC CCTAATAATT ATAGCAGGGC CCAAGACAAG 180 TCTTCCCGAG CCCCACTGCA GAAGCAAGAA CGGGGCCCCT CTCAGGCCTG GCACAGGTCT 240 CTGTCATGCT TATGTGTGTA ATTCAAATGT CATGGTTCCC AGATAGAAGC CCTCAAAGGT 300 CTGAAGGCTG GGCCTGTACT GAGGCTGACC TCTCAGGAGG GGAGAACTCT TGCAGCCCTG 360 GCCGGCAGGA AGGGCCTCTG TGCAGGGGCT TGTGTACATT ACAAGTCATG CTGGAAGAAT 420 GCCCGTCTGC TGGACAATCA CTTGCCCGTT ACAGCCCCAT CCTGGAGCTT GACCTCATTC 480 CTCGCCTAGG GCCTGGAGGA CATGGAGAAT TGAAAACAGA TCCTGATCCA AAAGTTAGAT 540 CTCTGGAAAT TTTGCAGTAG CTGTCTATAA ACCACCTGCT TAGGGATGAA CGCGATCTCT 600 ACTGGTCCGC TGCCCTCTGT GTGAGCCGGT GGTGTTATAC ACGGCAGTGA CGCGCAGCCC 660 GCCACTGCCC CCGTGGCTGG GCTGAGTGCC CGTCTCCTAC CTTCCCCTCG AGCTCGGTGC 720 GCAATCGTCA CCATACAGCC CCCACCACAG ACACCACACT CAGCAGGCCT GGCGCTCACA 780 CGCTTACAGT GCCAGCCGTT TCCAGGGACA GCAAATGAAC CACCTACCCC TCCTTCAGCT 840 ACAGGCTCCA GCTGGCCCCA GGATCAGGGA GGCTGAGCCA CAGGCCAGGG AGAGGAAGTG 900 GCAGAAGGAG ACCAAAAGAA AAATCATAAT TGAAGTATCA GGTCTCCAGC ACCCCATTCT 960 TTTCCTCTGA CATTCATGCA CCCCAGAGTG TAAGAGCGAT TGTCTGCAGT GAGTTAAACT 1020 GGAGGCACTG GGACACTGTT TCTATGGCAA CCCCTCTCGG CTCTAATTCA GCTCTGAGTT 1080 AAAAATGCTA TCAAATAATT GGAGAGTGCA GGAAAGCACA GCCAGCAGCC TGACCCCCTG 1140 TCCCATCCTT CCTAGACCTT CAGGTGTACA GGAGCTGAGA AGGCCCCCAT CACGTGGGAG 1200 CAGCACAGGC GCAGGCTTGG CTGGGAGCAC AGAACAGTCT GTAGGGAGAC GATTTCGGAG 1260
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