Tag | Content |
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EnhancerAtlas ID | HS095-06024 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr11:102700060-102701460 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr11:102700713-102700725 | AAACAAACATTT | - | 6.27 | OLIG2 | MA0678.1 | chr11:102701400-102701410 | ACCATATGGT | + | 6.02 | OLIG2 | MA0678.1 | chr11:102701400-102701410 | ACCATATGGT | - | 6.02 | Stat6 | MA0520.1 | chr11:102701223-102701238 | CATTTCCTAAGAATT | + | 6.13 |
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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 | TTTGTGCTGC TTCCAGAATG ATTCTACCCA AATCCCAGGT GGTTAGCAAG CTGGACTTTT 60 TCTCATAATT AAACCCTGCC AACTTCTTCA ATTTTACAGA AAATTGCTTT CACAAGTTAT 120 TCCTGCCAGA TCTGAGTAGC TTCAATGCAC TCTTCCCACA GTGCTCCTTC ACAATAGGAT 180 CACGGCTAAT CTCCATATTG CTTGATTTGT GATAATAGGC TTCTTAAATG CTTCTGTCAT 240 TATAACCCAT CTGCTCACTA ACTGGTGAGA TTCTGTACTT TATCGTTTAT GAACGTTCTT 300 ATTTGTGTCA AACCCATATT TCTGTTGGTT TATTGCTGAG TCCAAACCAG ATTCCCAGCT 360 TCTGCTTTCC TCCCCTGCCC CCCAGTCTAG TGTCCCTCCC CCAGTCTAGT GTCCCTCCCC 420 CAGTCTAGTG TCACTGCATG ATTTCCTGTA AATGCAAACG TACTCCAATA AGCCTGCCTG 480 AAGCAAGAGG AATTGAGCCA GCTATCAAAC ATCATTCTGG GATTCAGCAT CAGTCACCAT 540 TAGAGCTGGT CTTGTCCCGA CATGGGCTAC ATGTCTGGTC CCTGGGGCTT AGCCTCTGGT 600 CGGTGTCAAA TTCAGGTGAA AGCCTTGTCA GCACAAAAAT ACATACCTGG AACAAACAAA 660 CATTTCTGGA ACAAGATTGC TTGGGGAAAT TTACAGACGA GTAGCTGGTG TGAGGTTCTC 720 CATTGTTCAT TACAATTTAG GACAGCACAA AGAAATTTAG CAGGGCTAGA TATCAGACTC 780 AAAAGAACCC CGGCCCTTGG GCTGTGGGGA TTTTAAACTG CAGAATTGAG GAAGAACCAG 840 CCCCAATGTG GTCATGCCAT ATGACACTGC AGAACCCCTA GTTCGGAATG GAGTCAAAAC 900 TGAAAAGATA AGGCAACCAG GCTGATTTAT TGTCTGGGTC CCTAGACAAA ATAAGAACAT 960 GATCTTTGAA TCTAGAAGGA TATGAAATTG GATCCTGGCT ATGTACTTGC TATGTGATTA 1020 TGGCAATGCT ACTGAATTAC TCTAAACTTA TATTTCTGCA TTATTGAAAT CAACTACCAG 1080 CCTAACAGTT AAGACATGCA TAAGAACTAT GAATCAGGTC TGATAGCACA GAGAAAGTAT 1140 TTTCCACTTC CTTCTCAGCA CAACATTTCC TAAGAATTAT TTGCATCTGT TATTTCGACT 1200 TTCTCACATT CCAGTTTCTC TTTGTAGTAG ATGGACAGAG ATTGGTGACT CAATGTCTTT 1260 CCTTCACCTC ACTGTGTAAC AAAAACATGA CTGCAGTGAA ATTGATTGAT CCTCCCTGCC 1320 ATGGTGATTG GTCTAGGATG ACCATATGGT AAGGGATGGT CCAAACAGGA GGACACTCAG 1380 AACTGTCCTT TCGTGTTTGA 1400
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