Tag | Content |
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EnhancerAtlas ID | HS101-02980 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:160782550-160783420 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr1:160783212-160783227 | CATGCTGAGTCATGG | - | 6.74 | Nfe2l2 | MA0150.2 | chr1:160783214-160783229 | TGCTGAGTCATGGTG | - | 8.73 |
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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 |
GH01I160813 | chr1 | 160783121 | 160783270 |
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Enhancer Sequence | CAATTTTTTT TAATGTATTA CCTATTCAAA AGAAGAAATA TTGGGCCAGG TGCAGTGGCT 60 CATGCCTGTA ATCCCAGCAC TTTGGGAGGC CAAGGCAGAC AGATCACCTG AGGTCAGGAG 120 TTCGAGACCA GCCTGGCCAA CTGGTGAAAC TTCATCTCTA CTAAAAATAC AAAAATTAGC 180 CGGGTGTGGT GCTGTGTGCC TGTAATCCCA GCTACTCAGG AGGCTGAGGC AGGAGAATCG 240 CTTGAACCCA GGAGGCAGAG GTTGCAGTGA GCAGTGATCA CGCCACTGCA CTCTAGCCTG 300 GGTAACAGAG TGAGACTCTG TCTCAAAAAA GAAATATAAC TTAATGAAAC ATTCACACAT 360 GTGCACATAC ATGGTGAGCA GTGGAGATGG AACAAAAGGA AAGGAGAAGA CAAGGAAGAA 420 GATCTAGAAG CACAATGCAT CCTAAATTCA GACCAAAGAC ACGGGCAACT CAAATTCTAG 480 AAGCAGAGGT CCCCACTCCA TAGCGTTTGG GGCTGGGCCA TTCACCTATT TATTCATTGA 540 ACATTCATGA GTGTTTTTCA TAAGGCAGGC TGGGTGTTAG ATGTTCAGAC ACAGGAATCA 600 GCCCTGTCAT CAAGGAGTTC TTACACTGGT CGGGGAGAGA GAGAAGTAAT CAGACTATTA 660 GTCATGCTGA GTCATGGTGA TAACACCTGT AGCGGATGTT ATGGGAGTAC AGAGGAGAGG 720 CTGTCAACCC AGCCTGCAGA GAAGATGTCC CTGCGACAGG TAACGCTGGC CTCTCTCTGC 780 TGCCCCCAAC TCCCCTATTG TCACTCCCTT CTTCTCTCAG CGCTTTCCTG CTGGCAAAAG 840 GATCTGAGCA TCTTCCCATG CTGTTGTCCC 870
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