Tag | Content |
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EnhancerAtlas ID | HS176-08361 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr11:122512790-122514290 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr11:122514239-122514254 | GATGTCAAGAGTTCA | + | 6.13 | Nr2f6(var.2) | MA0728.1 | chr11:122512862-122512877 | TGAACTCCTGACCTC | - | 6.22 |
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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 |
GH11I122641 | chr11 | 122512322 | 122514653 |
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Enhancer Sequence | GCACCATCAC GCCCGGCTAA TTTTTGTATT TTTAGTAGAG ACAGGGTTTC ACCATGTTGG 60 CCAGGCTGGT CTTGAACTCC TGACCTCAAG TGATCCGCCG GCCTTGGCCT TCCAAAGTGC 120 TGGGACTACA GGCGTAAGCC ACTGTGCCCA GCCGGTGACA AGTTAACTTT AGTCTCTTTC 180 CACTATCTCT TGTTCATAAC AATTTACTAG TCCATATATG TACAGGTGTA AGCCACTGTG 240 CCCAGCCAGT GACAAGTTAA CTTTAGTCTC TTTCCACTAT CTCTTGTTCA TAACAATTTA 300 CTAGTCCATA TATGAGATGT GATTATGAAA TAAAGAACAA GATCGATATT TCATGTAACT 360 ATACTGAAAT GAAAACATCT AAATCCCTGC CATCCCCAGC ATAGCAGTAC ATCTTGGGAA 420 GCTACCCACT TGGCCTAACT CCACTCACTG TGTTTGCTCA AAACATTTTT GGAATGCTTC 480 TCTCTGCCAG TCAGAGCCCC AAGCAGAAGA CATTCACAGG AAATGAAATC AATGATTTAC 540 TATTCATCCG CCATAGACTG TTACTCATCC TGAACAAGTG AATGAGTGAT TATTTTCAAA 600 ACAGACGAAC AGATAAGAGC AAGCCACAAC CCTCACACCA CTTCACAGAG TGGCCATTCA 660 GCACTCAGAC CAAGTATCCC TCAGCTTCCC AGAACTTTTT CCAGATACGC TCAGAGAAGC 720 ACTTGTTGGC AACTTCACCA GGAGCCACTT TCTAAATGGG GAAGAGATTG GCTCTGAGGA 780 ACAGCATGGA TTAGTCACAG GAGGCGAGGG ATGGTGACAT TCCTGAAAAC AGAGGGGACC 840 AGAAATAGAT TTACACATGT CTAGGGCACT CTTTTCTCTA CAGAAAGGTT TAAAAACACT 900 GGCTCTAATG AGGGGTGGGT GGTATGTAAC AAGGGTAATG TGGGAGAGAG GCAAACCCAT 960 TTCAGGGAAA AGCACTTCCC TGGAGATGTT CTCAAGAGCC TTTATTTACA GAAAAAGTTG 1020 CGTGACCGTG AGCATCCTGA AGAAGAACCA CCTTCCTCAG ATTTCAAAGG CCAATCATGT 1080 TGATGCTCTT AGCCAGTGAT TACTAGCTGG ATCTGTGGAT TTGTGAGACG CCTGTGTGGT 1140 GATGTGAAAA CGGAAAAGTC CAAGAACCGG AAGCCAAGCA GCTTAGACGG CTCTGGCACC 1200 TTGGGGCCAG TGCTAGGCAC TCAGAGTGAG AGCATCCCCT GCTCAGGTGA AGTAATCTTT 1260 CCTGCAAGGC TCTACAACCA CTGGAGAGAG ACCCAAGGTC CTCCGTCATT TGAAAGGCTT 1320 AACTGCAATT TCTTTTTTAT TTTACTTTAT GTCTAATTTT TAAAATAGAA ACAGGGTCTC 1380 TCAGGCCAGG CGCGGTGGCT CACGCCTATA ATCTCAGCAC TTTGGGAGGC CGAGGTGGGT 1440 GGATCATTTG ATGTCAAGAG TTCAAGACCA GCCTGACCAA CATGGTGAAA CCCCGTCTCT 1500
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