| Tag | Content |
|---|
EnhancerAtlas ID | HS177-04685 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr11:116298310-116299570 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESRRB | MA0141.3 | chr11:116298457-116298468 | TCAAGGTCATT | + | 6.32 | | Esrra | MA0592.2 | chr11:116298456-116298467 | CTCAAGGTCAT | + | 6.02 | | Esrrg | MA0643.1 | chr11:116298457-116298467 | TCAAGGTCAT | + | 6.02 | | Gata4 | MA0482.1 | chr11:116299290-116299301 | GGGAGATAAGA | - | 6.62 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_63251 | chr11:116282793-116299761 | GLC16 |
|
| | 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 |
| GH11I116426 | chr11 | 116297369 | 116300113 |
|
Enhancer Sequence | TGTGAGGGCC CAGGGATCTA GAATCCTATC TAAACCCCAG GCCTAACTAT CCCTCAATTC 60
TACAATGTCA TAGCTTGGGA GCCTAAAAGC TGGACAGAGT CGTCTCCTCT GAAATGGCCT 120
AGCCCCTGTC CTTTCAGAGA GAGCTTCTCA AGGTCATTGC AAAACCAGGC TCTCAAGGCC 180
CCTCCCTACA GCCTCGGCTT TCCTCTCTAG GAGCAAAGTC CCACCAAGAC CTGAACTCTA 240
GCTGCAAGAA TTCAAGACGT GTTCAATTCA CTTCCAGGTT CTCCTCCCAC CCACCACCAG 300
CCCTCTATCC CCCAGAGCTA GGCAGCAGCT GCTGTTAGGA GATCCTATCC AGCCCTGGCT 360
TGACATTTCA ACAGCCCGAG ACCCAGAGAT AAAAGTTGTC ACTGAACAAA GTTCATCCCC 420
CTCTCCCGCT CCCTTCCTGG AGCCTCGATA GGCATCAGAA TGGGCACTGA GATGGTCTCT 480
CTTGCTTTCT ACTGCTGCTG CCGCTGCTGC AATTCCTGCT TTTTATTTAG AGGGGTGGGG 540
GGAGATTTCA CAACTGATGA TTACGAAGAA GCGGTTTATC ACCTGTGCTT TTATGATTGT 600
AGCGACTAAG GGGAAAAAGA TGTCTTTTCA GATAAGCATT TGAAGGACGG GGAGAAAGAT 660
TTTCAAAGCT CCCTTTGTTC TCCTGGAGGG CCACGCCATT GAGTTCTGGC AGGCAGCCCG 720
GGAGAAAGGA GGATTTTAAA AACACAATCT GAGCTGGCTT CCAAACCCCT GCTCACCATC 780
CCTGTCATCA ATTAGGGATG TTACTTAACA AGGGGTTTGG GCCATTGTCT CATCCAGCCT 840
GCTTTCCCTA ATTGGATGCA GAGTGGTGAT GAATTATTTG GAAAAGGGCT CCACACTGCA 900
GAGGTCATTG CTTTGGCCCC CTGACACTCA AGGCCAGCTC AGGCTGGGCT GGTGTGGGCC 960
TCTGGGGCAT GTTGCTGGCA GGGAGATAAG AGAAGGACCT TTCTGAGGCC CCTCAGTGCA 1020
GGCGGAGAGC ACAGACCCAG AACCCAGAGA AGGGCAGGCT GCCAGTCCAT GCGGGGAACT 1080
GAAGGTGAGT GGCCAGGGAG AAGATGGGGG CCGCTCCTGT GGCCTCTGCC ACCCCCAGCC 1140
CCCACTCCAG TTTCTGAAGA TGGAGCTCGG TGAGCACAGA GAGCTTTAAG GCCTCAGTCC 1200
ACAAAGGGAC GGGTCTGAAT TCGTTAGGTC AAACTGCCAT AGACTCATAA ATATTGTGCC 1260
|
