| Tag | Content |
|---|
EnhancerAtlas ID | HS091-43724 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr7:45006440-45007200 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr7:45006698-45006716 | TCTGCCTTCCTTCTCTCC | - | 6.33 | | EWSR1-FLI1 | MA0149.1 | chr7:45006702-45006720 | CCTTCCTTCTCTCCTTCC | - | 8.16 | | KLF14 | MA0740.1 | chr7:45006660-45006674 | AGGTGGGCGTGGCA | - | 7.14 | | NFIA | MA0670.1 | chr7:45007137-45007147 | ACTTGGCACC | - | 6.02 | | SP3 | MA0746.2 | chr7:45006661-45006674 | GGTGGGCGTGGCA | - | 7.12 | | SP8 | MA0747.1 | chr7:45006661-45006673 | GGTGGGCGTGGC | - | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr7 | 45006600 | 45007000 | | chr7 | 45006664 | 45006966 |
|
Enhancer Sequence | CAGGGACAGA GGGGACTTGG AGAGGGTCTG CGCCAGCAGC ACTGTGCACC CTGCCCCACA 60
CCAGGGGCTT CCTAACCCCT CAAGGTCCCA GGCCAGGAGA AGAGTTGGGA ACAAAGAAGG 120
GAAATCAGCA GAACAAGGGC CCTGGAAGCC CTAAGTGCTG GGCAGAGGCC AGCAAGGCCA 180
GGTTCAGAGC CAGGTTCCAG CCCCTGGTCG GGGGGTGGGG AGGTGGGCGT GGCAGGGGCA 240
GGAGCAGGCC TCGCCCCATC TGCCTTCCTT CTCTCCTTCC AAAAGGGGCT GACATCTCTG 300
GATGTTCTGT AGTTAAGCTC ACCCTAACAT GTCCTCTCCC TGACCCTTCA CCTGTTCCTC 360
TTCTGACTTT TGACCCAAAG CTCCCCAAGA AAGCTTGTGC CAGTTTCCTG TCTCTCTGGC 420
CCCACCTGCC AGAAGAATCC TGGGTTTTTG CCAAGAGCTG GGCTGGGCCA AGCCAGCCTC 480
TCAGCAGGGT CTCCCCAAAC CCCTCCCTGT TCAAGAGACA ATGGGGCGAG GAGAAGCCTG 540
GGTTCCCCAT GATTGATCAA GCCTCAGCCC AGCCCCTGAG GCCCCACATC TCACCTGTGC 600
AGTGGGTGGG GTCCACTGCT GGAGCAGATG TGGCTCATAC AGACAGGACA AGAACCCTCT 660
CCCCACCACT ATGATGTACA GAGGTGGTTG GGACCCTACT TGGCACCGAG GGCACAGAGA 720
GAAGGATCCG GAACAGCCAG AGTGGGAGAG GGGTGGAACA 760
|
