Tag | Content |
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EnhancerAtlas ID | HS108-40836 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr9:90381540-90382480 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXH1 | MA0479.1 | chr9:90382321-90382332 | TGTGGATTGGA | - | 6.62 | SP1 | MA0079.4 | chr9:90381729-90381744 | GGGGGGCGGGGTCAG | - | 6.2 |
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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 |
GH09I087766 | chr9 | 90381432 | 90382482 |
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Enhancer Sequence | ACTGCATCTC AAAAAAAAAA ATTATTAAAT GATACCTGTT ACAGAATGAT AAGAAATAAT 60 TTATTTAGGT CCTTGAGGTA GGTATAGGGA CCACTGGAAG GAAGTCTTGC AATGAGAAGG 120 AGAAACTGGG CTCAACTCTG AATACAGCAT GGGCAAGCAG GAAATTATAG CCAAGGAAAA 180 GGGTGGGGTG GGGGGCGGGG TCAGTGGATG GGAAATGACT ATGTGGAAAC ATCAGGGGTA 240 AGGGAGGATT CTGGCTAAAC TCACCTAACA GGATTCTTGC TGAGGACAAG CCAAGGCTAT 300 CTGACATCAC CTGGAGGATG GGGGAGGCTG AGGACTCTGA TCAGATATGA AGAATGGGGA 360 TTCTTGCTAA ACTGACTTAG CAGGTTTCTT TGCTAAAACT GAAATTTCAC AAGGAAGTGC 420 ATAGATGAGT CTAGCACAAC ATTAAGAAGC CTGACTAAAG TCTGGTCAAA CAAAACATTT 480 TCTGTCACCA CACAGAATGT ATGCTGCTGG AAACAGACTG GGCCTCAGCA TCTTCCTACC 540 CCACCAGCTT CTGGGAGGGC ATTTTGCCCT GTGCCTCCTG GGTGTTTCCT TGCTTGATCA 600 TGTCTAGGAG ACAAAAGACT TGCACCTTAT CATTTATGAT AAATTCAGTG TCAGATTTTT 660 AATACTAAAT CAGGTGACAA TGCTTCAGTG AACAATCTCA GGAATTAAAA TAATGAAGTT 720 CATTCATTCA CCAATTCTTC GTGTGTGTGT GGTTTAAGAC AATTTATTTT GCTCATGATT 780 TTGTGGATTG GAGCCCAGCC ACATTTGATA AGATGGAGAA ATGGATTCCA CCTCTTGAAG 840 ACAAGCAGGA GCGTCACAGT ACAGAACAGC ATACAGGCTG GAAGAGATTT CTGCAGCCAT 900 CTTTGGAGAA TACAATATGC TGCATACGTT ATTAAAGATT 940
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