Tag | Content |
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EnhancerAtlas ID | HS147-00818 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr1:26698130-26699150 |
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 | GGCATGACTA GGCCAGGTGT GGTGGCTCAC ATCTGTAATC CCAGCACTTT GGGAGGCTGA 60 GGTGGGCCAA CTGCTTGAGC CCAGGAGTTC AAGACCAGCA TGAGCAACAT GGTGAAACAC 120 CATCTCTACA AAAAATACAA AAATTAGCCA GGCATGGTAG CGCATGCCTG TTGTTCCAGC 180 TACTCAGGAG GCTGAGGTGG GAGGATCACT TGAGCCAGGG AGGTCGAGAC TGCAGTGAGC 240 TGAGATCATG CCACTGCACT CCAGCCTGGG TGACAGAGCG AGACCCTGTC TTAAAAAAAG 300 TTAATAAATA AGGAAAAGAC ATGTCTAGAT ACAAAAAGGG AGACCTCATA GGCCAGAAAG 360 TGGCTTTTTA GCCTGAGCAA TGTCATTATT CTTGTGAGCA TGAGAAGAGG CATCACCCCT 420 GCGGCCTTAC ACAAATTCTG GTGTGCGTGA GTCTGGCCCA GGGTGCAAAA GCCCCAACCA 480 GCCATCAATC TGCACCCCAG CCACGCCACC CTGGTGTCCC AGAATATACA GGGACATCTC 540 AGGCTGTGCA CCATGGGCTG GGGCATGTTC CTGGGGTTTC TCTGCCAGCT CAGCCCCTAG 600 GGCTGTGACT CATCCTCCAC ATAACTGATC CCAACATGTT TGTGAGCATC TCAAGGACAG 660 GGTCCTCTGT CTACTCATTT TGGTTTTCCA TGTAGACATC TGTCAGGTTT TTTTGGACGC 720 CCAGCCTCTG AAACTTTTCC CCTACATGAG TCTTGAGGGA GGCAAAAGGT ACCTCCCATT 780 ATAAAAGCCG AAATGGCCAA ATACTTAATT CCAACCTCCC TCACCAGCAC TTCATGCAGG 840 CATACATGGA CTAGGTCGAT CAGATGTCCC CACCCAGAAG GGGTGACCCG CACACCTTTG 900 GCTTCCATCT GCCAGCTCTG CCCTCTCCTG GCATCACACT CTGCTCCCAA CTCTCAGAAC 960 ACCTTGCACA ACTTCTCTGT TAGAAAAAAA TAAAAACTAC TTCCCCTCTA TCCGCACTTC 1020
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