| Tag | Content |
|---|
EnhancerAtlas ID | HS091-36332 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr4:8412080-8413200 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr4:8412613-8412631 | GGAAGGAAGGAACGCATG | + | 7.33 | | EWSR1-FLI1 | MA0149.1 | chr4:8412605-8412623 | AGAAGGAAGGAAGGAAGG | + | 9.09 | | EWSR1-FLI1 | MA0149.1 | chr4:8412609-8412627 | GGAAGGAAGGAAGGAACG | + | 9.45 | | SP1 | MA0079.4 | chr4:8412361-8412376 | CTAACCACGCCCCTT | + | 6.36 | | SP4 | MA0685.1 | chr4:8412361-8412378 | CTAACCACGCCCCTTAG | + | 6.08 | | ZNF263 | MA0528.1 | chr4:8413140-8413161 | TGAGGAGAAGTAGGAGGTGGG | + | 6 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_27420 | chr4:8412324-8413023 | Esophagus | | SE_37619 | chr4:8410514-8412871 | HSMMtube |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH04I008410 | chr4 | 8412224 | 8413092 |
|
Enhancer Sequence | TCCTGCACAA GGGAAAATTT AGGTTAGTTA TAATTAGCAA CTAAAGCACA TGCAGAATTG 60
GTGTTTTCCT TTTAGACAGA TTCCATTTTC TACGTTCAAA ATCTCTGAGG CAAGAGTTGA 120
AACTAATCGC ACATTTTAGT TCTTGTATGG CACAGGCAGG CCTATTTTTT AAACACAGCC 180
TATTCCTGGG CCTTATGACT TAAAGAACCT TCAGATGCAA AATACTCCGC AGGCTGGCAA 240
ACGCTTCCAG GGAGTTTTCA TTATCATATA GTCTTCAGTC CCTAACCACG CCCCTTAGGT 300
AGAAACACTG TGGATACACT GTGGGCGGAG CTGTCTGTGC ACTGTGGGCG GGGCTGTCTG 360
TGCCCTGTGG GCAGGGCTGT GGGAATGCCG TGCAGTCCAC TCAGTTCTTT AGGACCTCTA 420
ATTCACAACA CACTGCTGCC CCCTTGCTGT CTCTCCCATC CACAGCTCCG TGATTGACAG 480
TTATATCCCA AATGCCCCGA GCACAAGGCA GCCGCTCAGA ACATCAGAAG GAAGGAAGGA 540
AGGAACGCAT GCGTGAACTA GCAGATGGGC TGTGGCATCA CAGCGTTCGG TGTTTGGCTA 600
GAAGGGGTGT GGACAGATCC CCAAGGAACA CTGAGGGTGC TGCATGGGTC AGAAGCGAAG 660
AGCACGTGGG AACAGGCAGG AGCTGGGCCG CTGGGGCTGG GCCTGCCCCA GGGGCGTCTG 720
CTGGGAGCCC TTCGAGTAAG GCTGGGAGGG AGGATGCGGA CCAGCAGTGC TGCATAATGT 780
GGCCGGGATC CGCAAGGGGA CAAAGATGAG CGCCTTCAGG CAGACAGCCC GCAGGTGGCC 840
CACAGAGCTG CCCTGGGCCG CCTCGGGAGA CACTGATCCT CCACGCGGAG CTTGCCAGTC 900
ACTGCTAGGG GCTGTCGTGG CTAAGTTTTG GTTCTGGTTC CAGCCCCTGC AGGGTGGGAG 960
GCTACAAAAT AACGTGCCGG GGAGGGCTTC CTCCTGTCTA ACCAGTGGGA TTCTGTAAAC 1020
AGAGTAGTGA ACAATCATCC TATAGATCCT GAAGTTTCAC TGAGGAGAAG TAGGAGGTGG 1080
GGTGGCTGCC AGCCATGCCT TCTGTTCTCT TCTCTCAGGG 1120
|
