Tag | Content |
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EnhancerAtlas ID | HS095-00587 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr1:26698050-26699150 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOS | MA0476.1 | chr1:26698733-26698744 | TGTGACTCATC | + | 6.14 | JUND | MA0491.1 | chr1:26698733-26698744 | TGTGACTCATC | + | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 26698629 | 26698775 | chr1 | 26699018 | 26699071 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I026373 | chr1 | 26698661 | 26698810 |
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Enhancer Sequence | ACTGCACTCT AGCCTGGGTG ACAGAGAAAG ACCCTGTCTC TTTAAAAAAA AAAAAAATAG 60 ACATAGCAAA ATGGGTGTAA GGCATGACTA GGCCAGGTGT GGTGGCTCAC ATCTGTAATC 120 CCAGCACTTT GGGAGGCTGA GGTGGGCCAA CTGCTTGAGC CCAGGAGTTC AAGACCAGCA 180 TGAGCAACAT GGTGAAACAC CATCTCTACA AAAAATACAA AAATTAGCCA GGCATGGTAG 240 CGCATGCCTG TTGTTCCAGC TACTCAGGAG GCTGAGGTGG GAGGATCACT TGAGCCAGGG 300 AGGTCGAGAC TGCAGTGAGC TGAGATCATG CCACTGCACT CCAGCCTGGG TGACAGAGCG 360 AGACCCTGTC TTAAAAAAAG TTAATAAATA AGGAAAAGAC ATGTCTAGAT ACAAAAAGGG 420 AGACCTCATA GGCCAGAAAG TGGCTTTTTA GCCTGAGCAA TGTCATTATT CTTGTGAGCA 480 TGAGAAGAGG CATCACCCCT GCGGCCTTAC ACAAATTCTG GTGTGCGTGA GTCTGGCCCA 540 GGGTGCAAAA GCCCCAACCA GCCATCAATC TGCACCCCAG CCACGCCACC CTGGTGTCCC 600 AGAATATACA GGGACATCTC AGGCTGTGCA CCATGGGCTG GGGCATGTTC CTGGGGTTTC 660 TCTGCCAGCT CAGCCCCTAG GGCTGTGACT CATCCTCCAC ATAACTGATC CCAACATGTT 720 TGTGAGCATC TCAAGGACAG GGTCCTCTGT CTACTCATTT TGGTTTTCCA TGTAGACATC 780 TGTCAGGTTT TTTTGGACGC CCAGCCTCTG AAACTTTTCC CCTACATGAG TCTTGAGGGA 840 GGCAAAAGGT ACCTCCCATT ATAAAAGCCG AAATGGCCAA ATACTTAATT CCAACCTCCC 900 TCACCAGCAC TTCATGCAGG CATACATGGA CTAGGTCGAT CAGATGTCCC CACCCAGAAG 960 GGGTGACCCG CACACCTTTG GCTTCCATCT GCCAGCTCTG CCCTCTCCTG GCATCACACT 1020 CTGCTCCCAA CTCTCAGAAC ACCTTGCACA ACTTCTCTGT TAGAAAAAAA TAAAAACTAC 1080 TTCCCCTCTA TCCGCACTTC 1100
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