Tag | Content |
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EnhancerAtlas ID | HS042-45867 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr8:81213010-81214390 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFIC | MA0161.2 | chr8:81213233-81213244 | TATGCCAAGTA | - | 6.14 | RARA(var.2) | MA0730.1 | chr8:81213093-81213110 | TGCCCTCAGGATGACCT | - | 6.48 | RREB1 | MA0073.1 | chr8:81213777-81213797 | CCCCCCACCACCACACACAC | + | 6.25 | RREB1 | MA0073.1 | chr8:81213784-81213804 | CCACCACACACACACACACA | + | 6.41 | RREB1 | MA0073.1 | chr8:81213767-81213787 | CCCCCCCTCACCCCCCACCA | + | 7.13 | ZNF263 | MA0528.1 | chr8:81213768-81213789 | CCCCCCTCACCCCCCACCACC | - | 6.14 |
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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 |
GH08I080300 | chr8 | 81212434 | 81214170 |
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Enhancer Sequence | AAGTTTTAAT AGCTAGACTG GCTCTTCCTG TCTGTGCCAG GGCGGCATGT GGTGCATGCC 60 AAGCCACAGA GATGCTCAGG CTGTGCCCTC AGGATGACCT AGTGGGAGAC AGCAGCACCA 120 CTGGTGGCAG AGAACCCTGG CATCAAGCTC TTTGGGAAGT GGAGCTCCGA TGATGTGCAG 180 ATCTGGCACT TGCTTGCAGG ATTACACTGC AGTGAAGGAG AAGTATGCCA AGTACCTGCC 240 TCACAGTGCA GAGCGGTATG CCGCCAAACG CTTCCGCAAA GCTCAGTGCC CCATCGTGGA 300 GTGCCTCACT TACTCCATGA TGACGCACGG CCGCAACAAC CGCAAGAAGC TCATGATCAT 360 GCGCATCGTC AAGCACGCCT TCGAGATCAT CCAGCTGCTC ACAGGCGACA ACCCTCTGCA 420 GGTCCTGGTG AACGCCATCA TCAACAGTGG TCCCCGGGAG GACTCCACAC TCACTGGGCG 480 AGCCAGGATC GTGAGACGAC AGGCTGTGGC CGTGTCCCCA TTAAGCCGTG TGAATCAGGC 540 CATCTGGCCG CAGTGCACAG GAGCTCTTGA GGCTGCCTTC CGGAACATCA AGACCATTGC 600 TGAGTTCCTG GCAGATGAGC TCATCAGTGC TGTCAAGGGC TCCTCCAACT CCTATGCTAG 660 CAAGAAGAAG GACGAGCTTG AGTGTGTGGC CAAGTCCAAC CGCTGATTTT CCCGGTTGCT 720 GCCCAATAAA CCTGTCTGCC TTCTGCCTTT TGGGACGCCC CCCCTCACCC CCCACCACCA 780 CACACACACA CACACACACA CACACACACA CACACACACA CACACACGAA GTAGCTAGAC 840 TGAAGATGGA GCCAAGTTGA AACTTGCGTC CCAGGCTCTT ATGATAGCAT CAGAGTTTGA 900 CTTAGGTTTA AAAAGCAGGC CAGGAAAAAT TTCAAAGTGG CAAGTCATGG GGCAGGCTTT 960 GCAGAGCAGT CACTGCTGTT CCTTCTGCTA TCCCAAAAGG GCTTGAAGAG TGAATTACAG 1020 ATAAACCACT GGGTAAATAT CTTGTTACTT TCTATAAAAT GTAAACGTAG CTAAAAGAAG 1080 CAACCATGAG GCTGAGGATG CATTCACAAA AGCTCTGGAA TATTATAGAT GAAGCAGATG 1140 GTTCCCTCAT AATCAAAAAC TCAGCCGAAA ATGTCTTTCT CTGGAGGAAT AGAAGTTCGT 1200 GTTTGTAGAT TCTGTGTAAT CATGTTGTAA CAGAGCTTGT TAAACGGATT CAGATGAGCT 1260 ATGGGTCGAA TCCTGTTCGA CCCATATCGA GCTATTGGTC AACAACTAGA AAAGGCTAAG 1320 CCTGATCAAA TGGTATTTAT TGCTCTTCTC TTCCAATTCC ATTATAGAAA GATTCCAACA 1380
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