| Tag | Content |
|---|
EnhancerAtlas ID | HS091-23050 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr19:6711210-6712260 |
Target genes | | Number: 17 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myog | MA0500.1 | chr19:6711740-6711751 | CCGCAGCTGTC | - | 6.32 | | Pou2f3 | MA0627.1 | chr19:6712174-6712190 | CTGTATGCAAATGACA | + | 6.98 | | ZNF263 | MA0528.1 | chr19:6711404-6711425 | GGGGCAGGGGAGAAAGGAGAG | + | 6.27 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GGTGGGGAAA GAGGGATGCC TGCTGGTCGC CGCCCGAGGA TACCCACACC CGAATCCCTG 60
AGACCTGGGA ATTGGTGGCC TTTCTTAACA AAAGGGGCTT TGCAGATGGG ATTAAGTTAG 120
GGATCTGGAG ATGGAATCAT TATCCTGGAT TATGTAGGTG GAGCTAATGT AATCATAAGG 180
GTCTTTATTA AGCAGGGGCA GGGGAGAAAG GAGAGACAGA GACAGAGAGA AAGAGAGACA 240
CTGGAAGATG CTATGCTGCT GCCTTTAAAG GTGGAGGAAG GGGCCATGAG CCAGGCCTTT 300
AGGGTGCCCT GGCGACACTG GAAAAAGCAA GGGAGCGAAC TTTCCCCCAG AGCCAGGACT 360
TCTGACCTCT CAAACTATAG ACCCATAAAT GTGTGTTGCT TTAGATCACT AGGCTGTGGC 420
CATTTCTCAT GGTAGCCACC GGAAATTCAC GCACATGCTG AGCACAGGGA GGGGTAAGTG 480
GGGTGCGCAG CCTGGGAGCT GCAGAGGGAC TGGGAGGCCA TCTGCAACCT CCGCAGCTGT 540
CATGAGACTT GCTTCCCTCC CAGTGAGGGG CAACAGAGCC ACGTGCACAG AAGCCAGGAG 600
AACTGAGACC ACCTCACAAC AATGGGCCTG TCCCAAACAC TACACAACCC TCCTTGTGAG 660
ATTCAGGCTC CTTCCCCCAT GGGAGTGGAA AGACTGTGCG TGGATGGAGC GCCTCTCCGT 720
GTAAGTGGAA GGAGCAGGGC ATGCAAGAGG AAGATTCCTG TTTCCTCAAA CTGCGGACCC 780
CTCCATGCAG ACGGCAGGAC CCCACTGTGC AGGACAGAAC CCCTCTAGGC AAATGAGAAT 840
GTCTATGCAA ATGGCAGGAC CCCACTGTGC AGGACAGAAC CCCTCTATGC AGATGAGAGT 900
ATCTCTATGC AAATGGCAGG ACCCCTCTGC GCAGGAGAGA ACCTCTCTAT GCAGATGAGA 960
ATATCTGTAT GCAAATGACA GGACCCCACT GTGCAAACAC CAGAACCCCT GTACCGTCTT 1020
CCCAGTGATG GGGTTCCGAG GCTGGGCCCA 1050
|
