Tag | Content |
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EnhancerAtlas ID | HS167-05269 | Organism | Homo sapiens | Tissue/cell | Retina | Coordinate | chr5:138773920-138775090 | 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 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CGTGAACCCG GGAGGCGGAG GTTGCAGTGA GCCGAGATCG CGCTACTGCA CTCCAGCCTG 60 GGTGATAGAG CGAGACTCCG TCTCAAAAAA AAAAAAAAGA ACATTATGAG ATTTTTTTTT 120 GCAATTTTTT TAAAGTTCAT TAGCTGTCAT CAGTTAGTTA TTTAGTCGTC AGTTAGTGTA 180 TTTTATGTGT GGCCCAAGAC AATTCTTCTT CCAATGTGGT CCAGGGAAGC CAAAAGATTG 240 GATACCCCTG GTTTAAAGGG AGAAGATTCA ATAACAACAC CTGCAGAATG TAAAGAGGGT 300 CATAAGCAAT ACAGTCAAAA GGGGCAGAGC ACTCATGTCT TCTCTGGAGG ACCTGAGAAA 360 GGCTTTAACA ACATCTTTCT TCCGCTTAAC ATCCCTCAGC TACCTCCACC CACTGCTCCT 420 GGACAGTCTT CCTCTAAGTC GGCCTGGCTA ACTCCGACGC ATCCTTCTTG TCACCATTTG 480 TAACACTTTC TGCAAGAAAC CTCCCTTGAC AGCCAGTCTG CGTTAGGTAC CTTGTAAGTG 540 TGCTCTCCAA ATCCCTGACC TTGCTGTGTA GCCCAGGCGT TTTGTATTAT TCGCCCGTTT 600 TGTAATTGGC TGTTCAGTCG TCAAACTCTC TCAGTGGGCT GCGAGTTTTG TGAGCTAAGG 660 GACCCATGTC AGTCAAATCC CCACTGCAGA ATCAGCATTA GGCGGGGCAC ACAATAGGTA 720 TTGGATCAAT ATTTTTTGCC TGACTGTAGG GTGGAAAAGG CTGGTCCTGA TGCCGGCTGG 780 AGCGACATGA TCAAACAGGG ACTGAAGGTC AGGTGGCCCA GTTAGGCGAA AGATAAGGGC 840 CAGGTTAGCA AGCTGCGGAG AGACCGCAGC ACCCCACGGG CCCTCCAGTC ACCTTGGCAT 900 GGGCGGGGCC TGACAGCTGC GGGCCCTGGG CGGGGCACGG GCGGGGGCGG GGCTGGGGGC 960 CGGAGGCAAC AAGTCGTCAC CGGTGACTCT GGGCTCGCGG TCGGTCCCCA GCTTCCCTAC 1020 CCCATCCGCA ACCCTACTCA GGCTCAGCAT CTTTTCACAG GCCTCTATCC ATCACCTCAG 1080 ACCCAGGATC TCAGCCCTTG TGCGTCTTCA GGATCCTCAT CCCTGATCTC TCCCGAAGGC 1140 CGCCCTATCC CTCCTTCAGG CGGGGACCTA 1170
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