| Tag | Content |
|---|
EnhancerAtlas ID | HS091-12647 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr14:24681040-24682610 |
Target genes | | Number: 52 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GSC | MA0648.1 | chr14:24681135-24681145 | GCTAATCCCC | + | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr14:24681991-24682006 | CGAACTCTTGACCTC | - | 6.24 | | Zfx | MA0146.2 | chr14:24681544-24681558 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GAGTCCAGTG GAGTAGGCCC AAATTTTGTG AAGGAAAAAT ATTAGCCACC AATCATTGAA 60
TACATAGTAT GTGCTAGAGA CCTGACTGTG TTATTGCTAA TCCCCAAATC TCTACAATGA 120
ACGTGCTATC TCTTCACTTT AAAAATGTGA AAACAACCAC AAAGATGTTA AAAATCACAA 180
CTAATAAGAG ATTGTGCAGG AATCAAGATG TGGCAGTATG AGTTCTAAAA CCAATATTCT 240
TTTTACTATT CCTAGCTGCC TTTCTTTTTT TTTCTTTAGG CAGAGTTTCA GTCTTGTTGC 300
CCAGGCTGGA ACGCAATGGC GTGATCTCAG CTCACCTCAA CCTCCGCCTC CTGGGTTCAA 360
GCAATTCTCC TGCCTCAGCC TCCCAAATAG CTGGGATCAC AGGCATGTGC CACCATGCCT 420
GGCTAATTTT TTGTGTTTTT AGTACAGACA GGCTTTCTCC ATGTTGGTCA GGCTGGTGTC 480
GAACTCCCAA CCTCAGGTGA TCTGCCCGCC TCGGCCTCCC AAAGTGTTTT GATTACAGGC 540
ATGAGCCACC GCGCCAGGAC TTCTTTTTTT GAGACAGAGT CTCGCTCTGT TGCCCAGGCC 600
AGAGTGCAGT GGCATGATCT CAGCTCATTG CAACCTCCGT CTCCCGGGTT CAAGTGATTC 660
TCCTGCCTCA GCCTCCCTGA GTAGCTGGGA CTACAGGCAC ACACCATCAT GCCCACCTAA 720
TTTTTTTTTT TTTTTTTGAG AATGGAGTCT CCCTCTGTCA CCAAGGCTGG AGTGCATTGG 780
TGCAATCTTG GCTCACTACA ACCTCCGCCT CCTGGGTTCA AGCGATTCAC CTGTCTCAGC 840
CTCCCCCAGT AGCTGGGACT ACAGGCGCGT GCCACCACAA CCAGCTAATT TTTTTTTTTT 900
TTTTGTATTT TTAGTAGAGA CAAGGTTTCA CCATGTTGTC CAGGCTGGTC TCGAACTCTT 960
GACCTCAGGT GATCCACCCA CCTCGGCCTC CCAAAGTGCT GGGATTACAG GCGTGAGCCA 1020
CCGCGCCCGG CCAATTTTTA TATTTTTAGT AGAGACGGGG TTTCACCATA TTGGCCAGGC 1080
TGATCTCAAA CTCCTGACCT CATGATCCAC CCACGTCGGC CTCCCAAAGT GTTGCGAGTA 1140
CAGGCGTGAG CCCCCGCGCC GGGCTAAGAA GGCAGTCTTT CTTCTTCACC TTAGATCCCT 1200
CTTGCCCAGC ACAAAGTATT ATAGAACAAG GTTTTGAAAA TGGCTGAAGA CAGCAGGAAA 1260
CTCGTCTTCA AGCCTGAACA GTGGGAGTCA GCACGATCGC CACGCCCTCA ACTCAAGTCC 1320
CCTCCCAGAT CTTGAGTTCT TCCCTCTGAG AGTGGGGGAG GACGGCGGAC GGGAACAAGG 1380
CGCCCCGACA TGGTGTGCCT TTTGGCACCG GCGATGAGCC TTGCTCCGCC ATCGGCCGCC 1440
GGGGTTTTCC AGTCAGCCTG TCTCCTGATT CTCTTCCCCT GCCCGGCGCA GCGGTCCGGC 1500
CGAATCTCGC CGGGGTCTCC TCTTCCCCTG CACCAGCCAG CGCCTCCTGG CTGGCCAGTC 1560
CCACCCTGGC 1570
|
