| Tag | Content |
|---|
EnhancerAtlas ID | HS059-35262 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr4:84469080-84470040 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFE2L1 | MA0089.2 | chr4:84469799-84469814 | GCGTGACTCAGCATT | + | 6.81 | | Nfe2l2 | MA0150.2 | chr4:84469797-84469812 | TGGCGTGACTCAGCA | + | 6.51 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_41484 | chr4:84467624-84470430 | Left_Ventricle | | SE_56111 | chr4:84468554-84470868 | u87 |
|
| | 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 |
| GH04I083547 | chr4 | 84468755 | 84470583 |
|
Enhancer Sequence | CAGCCTCCCA AAGTGCTGGG ATTACAGCCA TAAGCCATAG TGCCGGGCCA TATCTTACTC 60
TTCTAAGCTT AAGGACTTTT CCTCATTGTT AACACAAAGA AAAAGGTAAA TCTTTTTCCC 120
CACTTCAAGT AACTCTGTTA TTCTGAGCAT TAAACTTCAG TGGAGGTTAT AGTTACCCTT 180
CTACCCTAGT TTTGTCCCCT GAAAGCAGAA GTGCTAGAGC CACAGCATAG AAGGCTAGGA 240
CAAGAAAATA CAGGAATAAT GGCTCGTTTG CTTCTTTTTA TCAGCTGTGC TTTGGTTGCT 300
CCAGCCATAG GACAAATGCA TCTCCTTGGA CCCTGGGACT TGGTCTGACT GAGATCCTAG 360
CAACTTTTAT TTTAGCCTGT TTTAAATATA CAAAGGATCG TTTGACTTTT AAGAGGCACC 420
AGCCTTACTC TTTGGGCATC TGATTTCCAG GGATTATGAT GCTGTTAGGT TGGAGTTTGA 480
ATCGGCTCAT AGCTTTGGTA GTAATTGTGA TTAATATTAG TAATTATGTA ATTTTAGTGA 540
CTCAAGATGA ATTGTACTCT AATTGCATTA TGACACTAGG ACATTTTAAA TGATTACCAT 600
GAAAAGTCAC CAAGCATGAA TAAAGGCCTG CATTTACCTG GGAGTGAGTC ATAAACACCA 660
CAAATACATA AAGGCGGTGG CTTGTCATTT TGGCATTGTT CCCTTAGAGG CTGATGCTGG 720
CGTGACTCAG CATTGTTGGC CACAAAGTGC ATGCAACCAC TGCAAGTCTT ACCCCATGCC 780
CTGCTCCAGC GGCACCACAC ACAAAGACTG TGGTCTCATG GCCTGCTGTT GATTTAGCCC 840
CTGTGCTAAA TTTCTCTCTG CCTTGTATCT CATGCCCCCA AGTCTCTGCC CCTTTGCCCA 900
CCTAAACACT CAAAAAGGAG AAGGTACTAA GGTGAAATTT CGGTTGCTAT ACCTATTTGG 960
|
