Tag | Content |
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EnhancerAtlas ID | HS197-17443 |
Organism | Homo sapiens |
Tissue/cell | ZR75-30 |
Coordinate | chr5:138774090-138775090 |
Target genes | Number: 13 | 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 | AGTTAGTGTA TTTTATGTGT GGCCCAAGAC AATTCTTCTT CCAATGTGGT CCAGGGAAGC 60 CAAAAGATTG GATACCCCTG GTTTAAAGGG AGAAGATTCA ATAACAACAC CTGCAGAATG 120 TAAAGAGGGT CATAAGCAAT ACAGTCAAAA GGGGCAGAGC ACTCATGTCT TCTCTGGAGG 180 ACCTGAGAAA GGCTTTAACA ACATCTTTCT TCCGCTTAAC ATCCCTCAGC TACCTCCACC 240 CACTGCTCCT GGACAGTCTT CCTCTAAGTC GGCCTGGCTA ACTCCGACGC ATCCTTCTTG 300 TCACCATTTG TAACACTTTC TGCAAGAAAC CTCCCTTGAC AGCCAGTCTG CGTTAGGTAC 360 CTTGTAAGTG TGCTCTCCAA ATCCCTGACC TTGCTGTGTA GCCCAGGCGT TTTGTATTAT 420 TCGCCCGTTT TGTAATTGGC TGTTCAGTCG TCAAACTCTC TCAGTGGGCT GCGAGTTTTG 480 TGAGCTAAGG GACCCATGTC AGTCAAATCC CCACTGCAGA ATCAGCATTA GGCGGGGCAC 540 ACAATAGGTA TTGGATCAAT ATTTTTTGCC TGACTGTAGG GTGGAAAAGG CTGGTCCTGA 600 TGCCGGCTGG AGCGACATGA TCAAACAGGG ACTGAAGGTC AGGTGGCCCA GTTAGGCGAA 660 AGATAAGGGC CAGGTTAGCA AGCTGCGGAG AGACCGCAGC ACCCCACGGG CCCTCCAGTC 720 ACCTTGGCAT GGGCGGGGCC TGACAGCTGC GGGCCCTGGG CGGGGCACGG GCGGGGGCGG 780 GGCTGGGGGC CGGAGGCAAC AAGTCGTCAC CGGTGACTCT GGGCTCGCGG TCGGTCCCCA 840 GCTTCCCTAC CCCATCCGCA ACCCTACTCA GGCTCAGCAT CTTTTCACAG GCCTCTATCC 900 ATCACCTCAG ACCCAGGATC TCAGCCCTTG TGCGTCTTCA GGATCCTCAT CCCTGATCTC 960 TCCCGAAGGC CGCCCTATCC CTCCTTCAGG CGGGGACCTA 1000
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