| Tag | Content |
|---|
EnhancerAtlas ID | HS091-47071 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr8:144918350-144919210 |
Target genes | | Number: 20 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr8:144918778-144918797 | TGGCCAGGAGGGGGTGCTG | + | 6.39 | | RREB1 | MA0073.1 | chr8:144918868-144918888 | GGGGGGGGGGTGGGAGGGGT | - | 6.75 | | ZNF263 | MA0528.1 | chr8:144918852-144918873 | GGGGGATGGGAGGGGTGGGGG | + | 6.21 | | ZNF740 | MA0753.2 | chr8:144918866-144918879 | GTGGGGGGGGGGT | - | 6.32 | | ZNF740 | MA0753.2 | chr8:144918868-144918881 | GGGGGGGGGGTGG | - | 6.44 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I143836 | chr8 | 144918307 | 144919330 |
|
Enhancer Sequence | CTGCAGCGGG GGAAGGCTGG GACTCACAAA CCCAGCAGCA AGACCACATG CCGCGGCCCC 60
AAAGGGGCCG GGAAGGGACA GCAAAGACTG GAAAGGGGGG AATCTCTAAG AGGAGCCCAT 120
CTCACTGCTA GTGGCTTGGC AAGCTAAGGA AAGCTTCGAG AAGAGTCGAC ATTAGGGGCT 180
GGGTACTGAA GGCTGAATAG GAGCTTTCAC CGCGGAGAGA ACAACTTGAA CAAAGAGGGA 240
ACTGTGGGCG TGGGGAAAGG GAGGTTGGGC GGGACAGGAC CGCGCCGAAG TGCACGGTGC 300
CTGCGGGATC AGGCCTCCCA GAGCCTGGGC GTCAGCTGAG GACTCCCATG ATCTCTGCTG 360
GCAGCCAGGA GCAGGCAGTT TGCCTGTTAG GACATGAATT CTGGCTGCAC TGCACCGAGA 420
GAGGCCCCTG GCCAGGAGGG GGTGCTGCAG GAAAAGTCTG GGGAGACACC AGGACATAGA 480
TGTCCGGGAA TCAGCACCAG GTGGGGGATG GGAGGGGTGG GGGGGGGGTG GGAGGGGTGC 540
GGGGGTGGGG GAAGATTGCT GGCAGGGTGG AAGAGCCCGG GTGAGTTCTG GAGGAAGGAT 600
GCTTGGAGTA GGTTCAGGGC AGGCAGCAGG ATGCAGGGGA AGGATCTGAG GGGACAGGGA 660
GCCTCCCGGA AAAGGAGAGT GCCCAGCCTG TCCTATAACC CCCATGACCC CCACAAGGGG 720
GTCAGCCTGG ATCTGGTCTC TGGCAGCCAG GAGGAGAGCT GGGCTGTGGG GATGCAGGCC 780
CTAAGAGAAG GAGGGGCACC TCTTATCTGG CTGTTAGAAG GTCTGAGGGA TGGCACTGAG 840
CAGCAGGAGA GGGGACTCAC 860
|
