Tag | Content |
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EnhancerAtlas ID | HS127-08021 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr12:110781240-110782690 |
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) |
TCF7L2 | MA0523.1 | chr12:110782590-110782604 | TGTCTTTGATCTTC | - | 6.41 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_26768 | chr12:110779806-110784507 | Esophagus |
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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 |
GH12I110343 | chr12 | 110781648 | 110784256 |
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Enhancer Sequence | TGAGTACAAT TTTTTTATAT TACTGATTTT TAAACAAAAT GTTTGTGAGC TGAAATTTTG 60 TAAATTCATC CCTTAAAAGC GTGTTTTTTC TTCTATCCCC GTATAGGGTA GCAAAAGACA 120 GAGATGCCCT CTTACAGTTC GATGAACTAT ACATCCAATT TACCAGAGTC CTTTCACAGT 180 TAGTTCCAGT TTTAGCATCC TGCCCTTACT TGGGCTTTTC TGAATGAGCA ATTAAACATC 240 AGGGTTTTCA GATTGAGCCC TCTGTGCAAA GGGATAAGAA TGATTCACGC TAGGTTCTGC 300 CTTCCAAGAG TTCATAGGTG GGATTTAAAT AGATAATTGT CACCAAGTTA TAAAATTTAG 360 TCCCTGTTTC CATAAGAGAA GGGTTGCGCA GTGGCTGGTC CCTTTTATAT ATAAATCATC 420 TCTTTAGCCC TCATCTTCCT CACCCCGGGT TCTTCCCCAT TTCATAGATT GGGAAAGTGA 480 GGTGAAATCA CTTCCCTGGG ATCCCATAGG AAGGCATTGT GTTTTCATAA TATATTCACA 540 TGACTTCAAA TTCAAAAAGC ACACAATGGC ATAGAATGGA AAGGGTTTGG GCCAGTCACT 600 TCCCTCTGGC GTTGAGGTGC TCATGTACCC TGTGCCCTTC CGGAGAGATT CCAGCATGCT 660 GTGCACACCT GCATGTTGAC CCTTGTCTTG CCTTCTTCCT GCTTGTCAGA TCCTTCCATA 720 TCCGGACATG CGTAGTGCCT CATCCTTGCA GCCAGCGGCC TTCATGCTCC ACTGTAATTC 780 GTGGGTTAGT GGGTATATGC ACTTGTTGTT TTTGATGCTA CCACATGGGG ATATTTGCCT 840 CGTCTGAACT CTGTGTATTC TCTGCTGCAC CTTGTTGCTT CTTTGCAATA AACTTCCTGA 900 ACTCAAAGCT AATACTGGGG GGAATCCCAG AAGCTGCTGA GGGCAGGGCC ATGCTGCTCA 960 GTGTTCCACC CTAGCTCCTG ACAGCATTTC CCTAGAAAAC TGCTGCTGGG CCTCTAATGG 1020 AGCAAATAAA TCTGTGTACA ACTAGGCAGC AATAGTTTGT CCAAAAGTCC TGGTGTAATC 1080 TAGTCCCTCA AACTGTGCAG CCTTACATGG AGTACACACA CACTTGCAGC CTTGAAGTAC 1140 TACCCACTGA GGGGAGAAGG CACGGCAAGG GGAAAGGTTG GCACAGGATG GAGCAAGTGC 1200 TTTTTCTCAC ACATTCTGGA GGAAAAGTTA TCCAGTTCTT CTGTTCTAGA AACACCCCTG 1260 TCCTTCAGAA ACCAGGGTCT AGTTGCTCTG GCTACCAGGC GTGAGCAGGT GGTGGTAGCA 1320 CCACAGGCCC CGGTTACCAT CACTGTCCCA TGTCTTTGAT CTTCGTCCTT GTGGGGACTG 1380 GCCTGCATGG CCTCGGTGGC AGCGAGCCCT GCAGAGGCAA GTGCATCAGC ATCACTGTGT 1440 TTGTTCCCAG 1450
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