| Tag | Content |
|---|
EnhancerAtlas ID | HS041-10826 |
Organism | Homo sapiens |
Tissue/cell | EWS502 |
Coordinate | chr2:15808710-15809540 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ELK1 | MA0028.2 | chr2:15809113-15809123 | ACCGGAAGTG | + | 6.02 | | ERG | MA0474.2 | chr2:15809113-15809123 | ACCGGAAGTG | + | 6.02 | | ETS1 | MA0098.3 | chr2:15809113-15809123 | ACCGGAAGTG | + | 6.02 | | FEV | MA0156.2 | chr2:15809113-15809123 | ACCGGAAGTG | + | 6.02 | | FLI1 | MA0475.2 | chr2:15809113-15809123 | ACCGGAAGTG | + | 6.02 | | ZNF263 | MA0528.1 | chr2:15809328-15809349 | GGTGGAGTAGGGGGCAGAGGG | + | 6.02 |
|
| | 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 |
| GH02I015668 | chr2 | 15808725 | 15808924 |
|
Enhancer Sequence | AGCCGACAAA ATATTCCCCA CACAATGACA AAAGCATATA CAAAGGTGGC TGAAACATAG 60
CTGGGTTTGA AATGCCTCTG TCTGTCCTGT CTGGGAGTGA GGCTGTCGAA TCCCTCCCCT 120
CCTCTGGGGA GGCTGTCTGT CCTCATGGGA GCCGCAGGTC CAATATTTTT GTGCTTGAAA 180
ACCCTGCCCT CGTCCACCCC AGGCGGCTCA CAGCTTTCAA CAGAGGATTA CTTAGAATAA 240
CAAGTTAATG ACTGTCCTTG GATTAGCTGA AGTTTGCTGG GAGAAGCAGA CATGCTCAGA 300
GTTCATTTCA CTCAAGTCTG ACGTGGGTGA GTTGAGAAAA CACGTTGCAA ATTCCATCCT 360
AGGAAAACAA GAAAAGAATT CTTCACGATG TCAAAGCAGC ATCACCGGAA GTGTGTGTGA 420
AAATGGAGCT TCCTTTAAAA CTATAAAAGC ATTTGTGCCT ATCTTCTGAG TGTGGCAGAG 480
TGTCTGGGTG GCAGACCTAC CTGGGAAATG ACAAGCAGGC CATGGGCTCT GTTGTTCTTA 540
GGGTCAAATG ATCTGGGGCC CCACAGGAAA CAGCTGGGGG TTTAAGTGTG AACCTGGAGT 600
GGGGAGACGT GGATCAGGGG TGGAGTAGGG GGCAGAGGGA GACAGAGGAG AGGCACCGCT 660
GACTCTACTC AGTCAACACC AGAGACCACC AACAGCCCAA GCTTCTAGCA GCTCCCTGCT 720
CCCAGCCCTC CAGCCAAACC TGTCTGATTC TCTTCTAGGT TCTGCAGGTG TCTATGCTCC 780
TTCATTCATT CACGCAATAA ACATTTGATG TCCTGAACTG ACTAGGGTTC 830
|
