| Tag | Content |
|---|
EnhancerAtlas ID | HS091-22926 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr19:4267770-4268580 |
Target genes | | Number: 28 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr19:4267813-4267832 | TGGCCTGTAGGTGGCAGCA | + | 6.98 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH19I004267 | chr19 | 4267721 | 4267910 | | GH19I004268 | chr19 | 4267985 | 4268797 |
|
Enhancer Sequence | GGTAAGGTCA CAGAGTTCCC AGAGCCGGGC GCGGTTTCTA TAGTGGCCTG TAGGTGGCAG 60
CAGCTCCCTT TGCAGTTACA GAGACTTCAT GGGGTGGGTG GGGGCGGCCT GCGACCCCCA 120
CAGGACCAAT TAGTGGAGTG AGCAGAGAAG GCAGGCGGCT TCTTTTTTTC TTTTTTCTTT 180
TTTCTTTTTT TTTTTTTGAG ACAGAGTCTT GCTCTGTTGC CCAGGCTGGA GTGCAGTGGT 240
GCCATCTCGG CTCACCGCAA CCTCCGCCTC CCTGGTTTGA GCAGTTCTCT GCCTCAGCCT 300
CCCAAGTAGC TGGGACTACA GCACCACGCC CGGCTAAATT TTTGTATTAT TAGTAGAGGT 360
GGGATTTCTC CATGTTGGTC AGGCTGGTCT GGAACTCCCG ACCTCAGGTG ATCCACTCAC 420
CTCGGCCTCC CAAAATGCTG GGATTACAGG CATGAGCCAC CGCGCCCGGC CTGTTTTTGT 480
CTTTTAGTTG CCTTAGTATG ATGTTTCCTA AGGCGATTAA GTCCACAGTG ACTGGACTGT 540
GAACTTTGCG CCATTTCCAT TCTTGGCAGC GCACGTTGCC TGCCTGGGCA AGGTTTGCAT 600
TGGCCATTGT TCAGAAGCGG AGCTGTTGAG TCCCGGGTGT GCAGATGTAA ATCTGCAATG 660
GGTCCCATCA GGTGCCATCC AGAAAGGCCA GGCCATTCAC ATGCTGTCAC CTCTGGACCT 720
TGCAAACCTG CAGAGGTGGC CGGCCCCGTG CCTTGTCCCT GGCCTGTCTG CTGTGGAGCT 780
GAGATGAGCT AACTCTCGCT CTCCCACCAG 810
|
