Tag | Content |
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EnhancerAtlas ID | HS127-15484 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr19:38778580-38779770 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CREB3 | MA0638.1 | chr19:38779624-38779638 | GGGTGACGTGGCAG | - | 6.73 | FOXP1 | MA0481.2 | chr19:38778676-38778688 | TTCTGTTTACTC | - | 6.27 | Tcf12 | MA0521.1 | chr19:38779293-38779304 | CAGCAGCTGTT | - | 6.32 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_26813 | chr19:38779171-38779907 | Esophagus | SE_31775 | chr19:38778435-38779880 | Gastric | SE_41685 | chr19:38778746-38779942 | LNCaP | SE_53909 | chr19:38778009-38779691 | Spleen |
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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 |
GH19I038287 | chr19 | 38778170 | 38779502 |
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Enhancer Sequence | TTCTTAAAGA GACCCGCGAT GGAGTGAGGC CACCGGATGG GTCATTGTGA AAGGACACTT 60 GTCATTTGGG AACTGTCACA GGCTTCCCTC TCATGGTTCT GTTTACTCAA AATTGGCAAA 120 CCGGGGGCTC TGCCTGGGCT GCCGGCTTCT GGCTCCAGCA TCCTTATGGG GGAGTTTATA 180 CTGTCCAGCT GACACAGGGG CCGGGGATCC TGCAGCACTT CCTGGCTGGC CCCCATCTCC 240 TCCTGGAGGA TGGGATGGAG GTGGCTGCTG CCCATGAGGC TCAGGCCCCT CCTTGCTGTG 300 CGGGCCTCCA GCTGCTCTGC TGACCCCACT CCCCACCCAC CCTCCTGTCT GCCTGTTCTG 360 TCTCCTCTGC TTCCTTTGCT CCCTGTTGCC ATCGCTGTCC CCTGCCCCGT GGGCATCCTC 420 TGTCCTCTGC CACCCCCGCC TCCCCGCCAC TGCAGCTTGT GATCTCAAGA TGTGTGTTAG 480 CTTGCTTTGT AGTGCTGGCG GCTGCTGCCC CATTCCTCCT TTATGGTTTA AGGACTCTGC 540 ATCGGGCGCC TGGGGTGAGT GGTCCCGATG CACTACCAGG TAGCAAATGC ACCCTCGGGG 600 CAGACCTCAG GCCATGGACT CTGGGAGGCT GCTGTGGAGG GGGTACTGCA CCGCACCCCT 660 GCTGGAGGAT GGGACTCCCC CGGCAGCTGC TACCCACCGA GTGCACTGTA GCTCAGCAGC 720 TGTTGGGCCG GCTGGCTTGC AGAGTGCTGG GGCGTTAGGG TGGTCACTTT CCAGCTTTGC 780 TAGGCCTGGA GTCCTGTGCC TGTCCTGGCT TTGCTCTGCC TGGCTCCCTG TTTATCCTCT 840 GCTAGCCCCC CCACACACCA GCTCTGGTTT CCATCTTGTT GGAGAGGAAC ATGTCCCCCT 900 CACTGTATTA GAAAGTGTGA ACAAGACCGT GTTCCCTATA ATATTAGGAG CTGTGGCAGG 960 CTTGGTTTCT ATAGGAACCC TGAGGTGGCG GCAGGGCCAC CACATCCAGC ACTCTCAGTG 1020 TGTGCGTAGA GCCCATTAGG GCTGGGGTGA CGTGGCAGAG CCGGCCATGG AAGGGGCTAC 1080 ACACCCCTTC TTAAAGGCGT GTCCACACTC CTCAGTGGGC CCTTCCAGAC CCAGACCCAG 1140 CTAGGCCTGT GTCCTGTGTC CGGCCCAGCC TCCCTAACAC AGATGTTTGT 1190
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