| Tag | Content |
|---|
EnhancerAtlas ID | HS091-39182 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr5:138774020-138775090 |
Target genes | | Number: 12 | 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 | ACATTATGAG ATTTTTTTTT GCAATTTTTT TAAAGTTCAT TAGCTGTCAT CAGTTAGTTA 60
TTTAGTCGTC AGTTAGTGTA TTTTATGTGT GGCCCAAGAC AATTCTTCTT CCAATGTGGT 120
CCAGGGAAGC CAAAAGATTG GATACCCCTG GTTTAAAGGG AGAAGATTCA ATAACAACAC 180
CTGCAGAATG TAAAGAGGGT CATAAGCAAT ACAGTCAAAA GGGGCAGAGC ACTCATGTCT 240
TCTCTGGAGG ACCTGAGAAA GGCTTTAACA ACATCTTTCT TCCGCTTAAC ATCCCTCAGC 300
TACCTCCACC CACTGCTCCT GGACAGTCTT CCTCTAAGTC GGCCTGGCTA ACTCCGACGC 360
ATCCTTCTTG TCACCATTTG TAACACTTTC TGCAAGAAAC CTCCCTTGAC AGCCAGTCTG 420
CGTTAGGTAC CTTGTAAGTG TGCTCTCCAA ATCCCTGACC TTGCTGTGTA GCCCAGGCGT 480
TTTGTATTAT TCGCCCGTTT TGTAATTGGC TGTTCAGTCG TCAAACTCTC TCAGTGGGCT 540
GCGAGTTTTG TGAGCTAAGG GACCCATGTC AGTCAAATCC CCACTGCAGA ATCAGCATTA 600
GGCGGGGCAC ACAATAGGTA TTGGATCAAT ATTTTTTGCC TGACTGTAGG GTGGAAAAGG 660
CTGGTCCTGA TGCCGGCTGG AGCGACATGA TCAAACAGGG ACTGAAGGTC AGGTGGCCCA 720
GTTAGGCGAA AGATAAGGGC CAGGTTAGCA AGCTGCGGAG AGACCGCAGC ACCCCACGGG 780
CCCTCCAGTC ACCTTGGCAT GGGCGGGGCC TGACAGCTGC GGGCCCTGGG CGGGGCACGG 840
GCGGGGGCGG GGCTGGGGGC CGGAGGCAAC AAGTCGTCAC CGGTGACTCT GGGCTCGCGG 900
TCGGTCCCCA GCTTCCCTAC CCCATCCGCA ACCCTACTCA GGCTCAGCAT CTTTTCACAG 960
GCCTCTATCC ATCACCTCAG ACCCAGGATC TCAGCCCTTG TGCGTCTTCA GGATCCTCAT 1020
CCCTGATCTC TCCCGAAGGC CGCCCTATCC CTCCTTCAGG CGGGGACCTA 1070
|
