Tag | Content |
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EnhancerAtlas ID | HS101-35772 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr5:138774350-138775090 |
Target genes | Number: 16 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF16 | MA0741.1 | chr5:138774862-138774873 | GGGGGCGGGGC | - | 6.02 | KLF5 | MA0599.1 | chr5:138774863-138774873 | GGGGCGGGGC | - | 6.02 | Myog | MA0500.1 | chr5:138774831-138774842 | GACAGCTGCGG | + | 6.32 |
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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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Enhancer Sequence | CCTCTAAGTC GGCCTGGCTA ACTCCGACGC ATCCTTCTTG TCACCATTTG TAACACTTTC 60 TGCAAGAAAC CTCCCTTGAC AGCCAGTCTG CGTTAGGTAC CTTGTAAGTG TGCTCTCCAA 120 ATCCCTGACC TTGCTGTGTA GCCCAGGCGT TTTGTATTAT TCGCCCGTTT TGTAATTGGC 180 TGTTCAGTCG TCAAACTCTC TCAGTGGGCT GCGAGTTTTG TGAGCTAAGG GACCCATGTC 240 AGTCAAATCC CCACTGCAGA ATCAGCATTA GGCGGGGCAC ACAATAGGTA TTGGATCAAT 300 ATTTTTTGCC TGACTGTAGG GTGGAAAAGG CTGGTCCTGA TGCCGGCTGG AGCGACATGA 360 TCAAACAGGG ACTGAAGGTC AGGTGGCCCA GTTAGGCGAA AGATAAGGGC CAGGTTAGCA 420 AGCTGCGGAG AGACCGCAGC ACCCCACGGG CCCTCCAGTC ACCTTGGCAT GGGCGGGGCC 480 TGACAGCTGC GGGCCCTGGG CGGGGCACGG GCGGGGGCGG GGCTGGGGGC CGGAGGCAAC 540 AAGTCGTCAC CGGTGACTCT GGGCTCGCGG TCGGTCCCCA GCTTCCCTAC CCCATCCGCA 600 ACCCTACTCA GGCTCAGCAT CTTTTCACAG GCCTCTATCC ATCACCTCAG ACCCAGGATC 660 TCAGCCCTTG TGCGTCTTCA GGATCCTCAT CCCTGATCTC TCCCGAAGGC CGCCCTATCC 720 CTCCTTCAGG CGGGGACCTA 740
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