Tag | Content |
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EnhancerAtlas ID | HS037-11662 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr14:59235150-59236550 |
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) |
MEF2A | MA0052.3 | chr14:59235231-59235243 | TCTATAAATAGC | + | 6.37 | MEF2B | MA0660.1 | chr14:59235231-59235243 | TCTATAAATAGC | + | 6.27 | Nr2f6(var.2) | MA0728.1 | chr14:59236072-59236087 | GAGGTCAAAAGTTCT | + | 6.07 | RARA | MA0729.1 | chr14:59236072-59236090 | GAGGTCAAAAGTTCTACT | + | 6.31 |
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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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Enhancer Sequence | TCACTGAGGC CTACAATCTT CTTTTCAGAT AACTTTTTCA TGTCATTATT TCTGTGTTAA 60 ATGGGGAATT AGATATTTTT CTCTATAAAT AGCTATCCCT GAAAAGTAGT ATGTACCTGC 120 TGAGTGCTTG TCACCAGTTT TAAATTAATT CACTGTTTTC AATGGATGAC TTTCCTAGTG 180 ATGCCACATA TATTTTAATA GCTGATGACC CTTTTGTGTC AGAACTAGAT ACCTGGATAT 240 CCCAAATCGA TGTAATGTTA GCCTGATGAT AATAATAGTA ATAGTTATAT AGTGCTTGCT 300 AGGAGTTAGA ATCTGCTTCA ACCACTTTAA TATAACTCAT TTTCATTCTC ACAATAATTC 360 ATGGAAGGTT GTATTTTTTT TTTCATTGTA CAGACGAAGA GGCTGTAATA GAGGTCAAGT 420 ATCAGTATGT TAAAACACCA CCTTTAGTTT TACAATAACT ATATAATTCC TCACTTTACT 480 CCCAAATCTT CACTAAATAT GGTGAACTCA TCTCCAGGCT AGTCATTTGT TGTGCAAACT 540 CACATTGATT TTTCAGTCTC TCAAAGTCAG AGCTGATAAT GACTTTGGCC ACCAACTGGT 600 TCGACTGCCC CCCACCTCGT GACTCTCTTC ACCAGACTTT TTAGGGAAAT CAAAAGCTTC 660 AGGTGAAAGC CTCAGCATAC TCTTCACCCT GCTTGAGTTG CCTTTCATCT AAATCTCTCT 720 AATGATAAGC TCCTAATGAG CTGATCTTCA CAATTGAAAT TCTGGCTTTG TTTTGCCGTA 780 TATTGTTGTG TTGGCGCTAA GGGAGGTCAC TTAGCACATG AAAATACCCC TTACCCCCTT 840 CCAGGCCACA GACTGTGGCC TATTTCATCC AGTGAGGCTG CTGGCTTTTG ACATGGAGTG 900 ATGGATGGAT GGGAGGGATT CTGAGGTCAA AAGTTCTACT TCCTTGCTGC TCAAAGTGTG 960 GTCCAGGAAC CAGGCAGCAT GGGTGTGATC AGGAAGCATA TGAGACATGC ACACACCCAG 1020 GCTCACCCCA CACTCACTGA ATCAGGATCT GCATTTAACA GGATTCTCAT TAACATTTGA 1080 GAAGCAATGT TCCACTCTAC AGTCCAGAGA ATGAGATTGC TGAAGTCCAT TTTAAGATTT 1140 TCCCCTTTTT CACTTGTGTT TCTCTCCTGT ATTCTCATCC CCAAGTGTCG AGAACAGATC 1200 TTGGCTTTTG GTAATTTCTC TCTTTAATAT GCATTACTGT AAGTCTTATA AATAAAAATA 1260 AATGTTCCCT TTTGGGTTTC ACACCTGTTC TTGCTTCATG AAATGTAATG TCTCCAGGCA 1320 GCTTACATTT AAAAAAAATT CTGAAATTCT GTGTGTGTTT CACAGTGTGA CACTATTTAT 1380 TTCTCTGAAG TTTTCAAAAA 1400
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