Tag | Content |
---|
EnhancerAtlas ID | HS060-28164 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr5:138774260-138775090 |
Target genes | Number: 16 | Name | Ensembl ID |
|
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 | TCTCTGGAGG ACCTGAGAAA GGCTTTAACA ACATCTTTCT TCCGCTTAAC ATCCCTCAGC 60 TACCTCCACC CACTGCTCCT GGACAGTCTT CCTCTAAGTC GGCCTGGCTA ACTCCGACGC 120 ATCCTTCTTG TCACCATTTG TAACACTTTC TGCAAGAAAC CTCCCTTGAC AGCCAGTCTG 180 CGTTAGGTAC CTTGTAAGTG TGCTCTCCAA ATCCCTGACC TTGCTGTGTA GCCCAGGCGT 240 TTTGTATTAT TCGCCCGTTT TGTAATTGGC TGTTCAGTCG TCAAACTCTC TCAGTGGGCT 300 GCGAGTTTTG TGAGCTAAGG GACCCATGTC AGTCAAATCC CCACTGCAGA ATCAGCATTA 360 GGCGGGGCAC ACAATAGGTA TTGGATCAAT ATTTTTTGCC TGACTGTAGG GTGGAAAAGG 420 CTGGTCCTGA TGCCGGCTGG AGCGACATGA TCAAACAGGG ACTGAAGGTC AGGTGGCCCA 480 GTTAGGCGAA AGATAAGGGC CAGGTTAGCA AGCTGCGGAG AGACCGCAGC ACCCCACGGG 540 CCCTCCAGTC ACCTTGGCAT GGGCGGGGCC TGACAGCTGC GGGCCCTGGG CGGGGCACGG 600 GCGGGGGCGG GGCTGGGGGC CGGAGGCAAC AAGTCGTCAC CGGTGACTCT GGGCTCGCGG 660 TCGGTCCCCA GCTTCCCTAC CCCATCCGCA ACCCTACTCA GGCTCAGCAT CTTTTCACAG 720 GCCTCTATCC ATCACCTCAG ACCCAGGATC TCAGCCCTTG TGCGTCTTCA GGATCCTCAT 780 CCCTGATCTC TCCCGAAGGC CGCCCTATCC CTCCTTCAGG CGGGGACCTA 830
|