| Tag | Content |
|---|
EnhancerAtlas ID | HS091-15974 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr16:1842520-1843630 |
Target genes | | Number: 39 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr16:1842606-1842616 | GCCCCGCCCC | + | 6.02 | | MYCN | MA0104.4 | chr16:1842657-1842669 | GGCCACGTGGGC | + | 6.27 | | MYCN | MA0104.4 | chr16:1842657-1842669 | GGCCACGTGGGC | - | 6.27 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr16 | 1842630 | 1842826 | | chr16 | 1843298 | 1843386 |
|
Enhancer Sequence | GATGCGAAGA AGCCGGTGAG CCCCACAGGT CCTCCGGCTC AAAAGCTGAC ACTGCGCTTC 60
CCACCCCATG GGACAGAGGA GTGGCCGCCC CGCCCCGCTG CACAGACGCT CAGGGCTTGG 120
CTCTCCAGCT GTGCGCAGGC CACGTGGGCT CGGCCAGGCT GGGTCTCGGG CTGTCTGGCC 180
ATGTGGCAGC CGCACCCCCA AGGCAGGCGC TTGAGCCAGG CCAGTCTGCC ACGTTGGCCT 240
AGAGGAAGGG GAGGGAACTG AGCCATTGGC CAAGGTCCGG CCATTTTCAG AATATTCTGC 300
AGCAGGTCTT GGTGGGCACT CGCTCACTGC CCTCAGAGGC TGGACAGGGA GCTGGGCACC 360
TCCTGCCCCA GTTAGGCCCC CCAGCGGGGT CTCACCTGCC TGCATCCAGG CCTTGGTCGG 420
GTGCTGCGGG AGGGGACCGG GGCACCGCCG TCGGGGGACA GGTAGGAACC CTGGACCGTC 480
GGCCACCAAA GCTCACATTG CCTTTCAGGA CAAGGGGCCA CAGGCCCCAC AGACCCAGCC 540
AGCAGGCTCC CAAGCAGCGA TGACCCAAAA CCTCTACTGT ATGGCCCCCC CATCCTCAGA 600
GAGTGTGGAA TTGCTGGGAT GGTGGCAGGG GCGAGGTGGG GCCCCCCCGA CTGCCCTTCT 660
GTCACGATGG GTTGGGAGTG GCCTGAGCCA GCTCTGGAGC TCAGCTCAGG CTTGGGGGTG 720
GCCGAAGCTG CAAGGGGTCA CCCCACAGAG ACAATGGGGT GTGAGCCAAC GTCTCCTGCC 780
TGGGCCGGGC CCACAACGCG GGCCGTGCGG GGCACTTCCC GCCGCTGTGC TGGGAGCTGA 840
AGGGTCCGGC CTGCACCTGG CCCTCCTCCC CTGTGCCGCC GCCAGCGCCC TTAGGGTGGA 900
GGACGGGACA GAGACCCCTG GTGCCAGGCA CAGCTGTGTC CCCCTGCCAA CCCCAGCAGC 960
CGCATTTCCG ACTGTGGGCT CCCCAGAGTC CCCCGCAGAC CCCCAGAGCT GAGCCCCCCA 1020
GAGCTTCCTT GGGGGCTACC CCGGCCTCTC CCCAGCGGGC TCAGGGTCAC AGACTGGCCA 1080
CCCCTAGAGT GGGTGGCGGG GCACTCGGGG 1110
|
