| Tag | Content |
|---|
EnhancerAtlas ID | HS161-01542 |
Organism | Homo sapiens |
Tissue/cell | PC3 |
Coordinate | chr1:223841230-223842030 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ELK1 | MA0028.2 | chr1:223841256-223841266 | CACTTCCGGT | - | 6.02 | | ERG | MA0474.2 | chr1:223841256-223841266 | CACTTCCGGT | - | 6.02 | | ETS1 | MA0098.3 | chr1:223841256-223841266 | CACTTCCGGT | - | 6.02 | | FEV | MA0156.2 | chr1:223841256-223841266 | CACTTCCGGT | - | 6.02 | | FLI1 | MA0475.2 | chr1:223841256-223841266 | CACTTCCGGT | - | 6.02 | | Myod1 | MA0499.1 | chr1:223841275-223841288 | TGCAGCTGTCACT | + | 6.78 |
|
| | 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 |
| GH01I223654 | chr1 | 223841653 | 223843699 |
|
Enhancer Sequence | AGCAGGATTT GTTTCTTTTT CACCTTCACT TCCGGTTCTG TATTTTGCAG CTGTCACTGG 60
ATGGTGGTTT GGAAGCCCCT CAAATTCAAT TCAGAGCCAT GTTGCCCATA AAATGTAAGG 120
ATTGTCCAAT TCAACGCAGA AACTCCCATC TGTGAAGCCT TGGTATCGGG AGGGCTTATG 180
AAATCAATAA AGCTCATCTG CCACCAAGGA GAGCCTCAGT TTCTGACAAT GGAGGCTAGA 240
ACTTACAAAA CTAAATGAAA TTATTTCTTA AAAACTCAAC TGCCCCTAAT TTAAAAGGAA 300
TATGATAAGT TCAGAAATGA AGGTTTTTGA TTACAGGATC CCAGGCCTAT GAAAGAATGT 360
CTGGCTACAA AAATAAGATT CCTGTTTTCT TACTAATTAT AAAAGCACTT ATTATGACAG 420
CCCATAATTA CTTAGATATG GCCATTCCAA AGGACAAATT ATGTCTACTT AAAGGTAACT 480
ACAACAAAAA CACAGTATAG CACAGATATC TACTCTACGC CTGTAATCCT GGCTCCTTGC 540
TCTAGCATTA AAGTGGTTAA ATGAACTGGC AAAATCTCTC ATTAGGGGGA GCCAAGAGGT 600
AGTTCCAGCA TTTGGACCTA CAGTGAAGTT CCAGCATTTG GACTCACAGT GAAGAATGCA 660
GTCTCAGAAA CACAAACCCA GACGGACACA TCAGGTACCT AATTCACTCG GTGAAGTCTC 720
ACAGCTTCAT CTGATGTTTA CTCATGACAC ATACACACCC GCCCTCTCCC AAAACAAATA 780
AGACTCTCCC CAGTTACTCA 800
|
