Tag | Content |
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EnhancerAtlas ID | HS093-12198 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr16:86016060-86016840 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nfe2l2 | MA0150.2 | chr16:86016094-86016109 | GAGGATGACTCGGCA | + | 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 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH16I085982 | chr16 | 86015661 | 86019930 |
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Enhancer Sequence | GGTGAATTGT GGTTGGGGGG AGCGGCTGGG GTGGGAGGAT GACTCGGCAG CTGCACTTTC 60 TCTGATTCTG CCAAGTCCCC CAGGAGCCTA GATGGACCTG TGAGCACCAG GGGCGGAGGA 120 CCCCGGTGGG GTGGGAACCA CCAGCAACAG GAAGAATCTG AAGGAGAGGA ACTTGGCAGA 180 AACCCGACTT CTCTAAAAAT ATTCAAAGCC CGTGGCCCAC AGAGGCTGGA TTGCGAGGCT 240 CCTGGGCTCC AGCAGCCGCG TCTCTGACCG TTGAGACCTG GCGCGGTCCA GGCGTTGAGC 300 AATAGGGCTG CGCCCGGTGT CATGCCCGCC GCCCACCCCG CCCTGCCTGC TCCACTTACA 360 CGGAGACGAG AGGCAGCTGC TGGTGTGGCC GCGTGTGCAT GTGGCCATGT GTGTCTATGT 420 GTGGCCATGC GTGTGTGAGT GTGGCCTCTC GTGTCAGTGG GTGGGCCTGC TGTCGGCTCC 480 TGCAGTCCCC TGTGGCCTCT TCTCCAAGGA CAGGTAGCAG AGCCCTCCTG TGAACCCAGC 540 ACAGATCCTG GGCTGGCTGT GGTCCGGGAG GGCCAGAGCA TAAGGGAATA AGTGTGGAGC 600 GCTTGCTCTA GGCCCAGCCC TGTGCTAAGC AGACCATAGC TGTAACCCAA GACACTATGA 660 GATAAGAACT ACTTTTGGCC CTATCGTACA GAGTCTGAGA TGAATTCAGA GAGGTCGAGT 720 TGTTTGCCTG AGGCCACACA GTGATGGGTG AAGCTGGAGG AAGCCAGCCT GCAGGGTGGT 780
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