Tag | Content |
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EnhancerAtlas ID | HS191-37324 |
Organism | Homo sapiens |
Tissue/cell | Trophoblast |
Coordinate | chr8:81212920-81214130 |
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 | TCCTCGTATC TCACGAAATT TGGGGAAGAC CCACGTACCT GAATTTTCCC AAAAGTTCCT 60 TAGGTGGTTC TGAACCACTA CTATGGTTGA AAGTTTTAAT AGCTAGACTG GCTCTTCCTG 120 TCTGTGCCAG GGCGGCATGT GGTGCATGCC AAGCCACAGA GATGCTCAGG CTGTGCCCTC 180 AGGATGACCT AGTGGGAGAC AGCAGCACCA CTGGTGGCAG AGAACCCTGG CATCAAGCTC 240 TTTGGGAAGT GGAGCTCCGA TGATGTGCAG ATCTGGCACT TGCTTGCAGG ATTACACTGC 300 AGTGAAGGAG AAGTATGCCA AGTACCTGCC TCACAGTGCA GAGCGGTATG CCGCCAAACG 360 CTTCCGCAAA GCTCAGTGCC CCATCGTGGA GTGCCTCACT TACTCCATGA TGACGCACGG 420 CCGCAACAAC CGCAAGAAGC TCATGATCAT GCGCATCGTC AAGCACGCCT TCGAGATCAT 480 CCAGCTGCTC ACAGGCGACA ACCCTCTGCA GGTCCTGGTG AACGCCATCA TCAACAGTGG 540 TCCCCGGGAG GACTCCACAC TCACTGGGCG AGCCAGGATC GTGAGACGAC AGGCTGTGGC 600 CGTGTCCCCA TTAAGCCGTG TGAATCAGGC CATCTGGCCG CAGTGCACAG GAGCTCTTGA 660 GGCTGCCTTC CGGAACATCA AGACCATTGC TGAGTTCCTG GCAGATGAGC TCATCAGTGC 720 TGTCAAGGGC TCCTCCAACT CCTATGCTAG CAAGAAGAAG GACGAGCTTG AGTGTGTGGC 780 CAAGTCCAAC CGCTGATTTT CCCGGTTGCT GCCCAATAAA CCTGTCTGCC TTCTGCCTTT 840 TGGGACGCCC CCCCTCACCC CCCACCACCA CACACACACA CACACACACA CACACACACA 900 CACACACACA CACACACGAA GTAGCTAGAC TGAAGATGGA GCCAAGTTGA AACTTGCGTC 960 CCAGGCTCTT ATGATAGCAT CAGAGTTTGA CTTAGGTTTA AAAAGCAGGC CAGGAAAAAT 1020 TTCAAAGTGG CAAGTCATGG GGCAGGCTTT GCAGAGCAGT CACTGCTGTT CCTTCTGCTA 1080 TCCCAAAAGG GCTTGAAGAG TGAATTACAG ATAAACCACT GGGTAAATAT CTTGTTACTT 1140 TCTATAAAAT GTAAACGTAG CTAAAAGAAG CAACCATGAG GCTGAGGATG CATTCACAAA 1200 AGCTCTGGAA 1210
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