| Tag | Content |
|---|
EnhancerAtlas ID | HS120-01228 |
Organism | Homo sapiens |
Tissue/cell | LNCaP-abl |
Coordinate | chr11:67905220-67906120 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr11:67905623-67905641 | GGAAGGAGGGAGGGGATG | + | 6.01 | | EWSR1-FLI1 | MA0149.1 | chr11:67905980-67905998 | GAAGCGAAGGAAGGCAGG | + | 6.03 | | ZNF263 | MA0528.1 | chr11:67905621-67905642 | GGGGAAGGAGGGAGGGGATGG | + | 6.19 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_08623 | chr11:67905288-67906295 | Brain_Inferior_Temporal_Lobe | | SE_23262 | chr11:67905346-67905662 | Colon_Crypt_1 | | SE_27927 | chr11:67905137-67906077 | Fetal_Intestine | | SE_31508 | chr11:67905280-67905779 | Gastric | | SE_35342 | chr11:67904926-67906390 | HepG2 |
|
| | 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 |
| GH11I068137 | chr11 | 67905084 | 67906181 |
|
Enhancer Sequence | CAACAAGAGC GAAACTCCAT CTCAAAAGAA AGAAAGAAAG AATGAATGAA TGAATAAATA 60
AATAAAATAA AAATTAAAAA AAGGTAGAAA CCCTTGCTTC CAGAAACTCC CCACTCCTTT 120
TGCAGAAAAC TCGTGAATAG CCTGTCCTTT ATTTAGCATA TAATGAAGGA ATAGACATAA 180
ATATAGCTGG CCAGCAATCC ACGAGGGCTG CCGCTACTGC TCTACGGAGC AGCCATTTTC 240
CTGCACTGTT GCTCTAATAA ACTTGTGTTT GCTTTGCTCT GTCTTGTTTG CTCACCCTTG 300
AATTCTTTTC TCTGCAAAGC CAAGAGCTCT CCCAGTCTGA GCCCCAATCA TCAAAGATGA 360
TTTTGAGGGC TTCAGTATTT AAAGGGGAAA AGCAGGCTGG AGGGGAAGGA GGGAGGGGAT 420
GGTCACATTA TTAAATCCGT ATGTTGGAAG AGAAAAGGAG CAGGGAGGGG AATAGTGACA 480
TATTCATCTA GTGCTTCTAC ATCGGCATTT TACACAAGAT AAGGTGAATG CAGAGTGTAG 540
ATATTTAACC TTTTATCCGT GGCTCTCTGC TTAGGAACAA AAGGAGAAGC AGCTTCTTGC 600
CTGACTCAGC TTTCAGCTTA ATTTTTTTCT TTTGGCAGAG TGAATTGGGA TTCCAAGATT 660
TTATTTGCCT TTCCCATCAT GCGATTGGAT ACCACAAAGC AGTGAAGAAC AGTGAGTGCC 720
CATGTACTTG ACAATGAAGG GGAATCTTCC AGACATACAT GAAGCGAAGG AAGGCAGGCA 780
AAAGAGTGTG CTTGTGTGAT ACTGCCTATT TGGGGCTCTA GAAGAGGCAA AACTAATCTA 840
TGGGAGTTTG AGGATAATGT TCAGGATAAT GGTTTACTTT TGGCAAGTGT TGTCTGAGAA 900
|
