| Tag | Content |
|---|
EnhancerAtlas ID | HS120-02849 |
Organism | Homo sapiens |
Tissue/cell | LNCaP-abl |
Coordinate | chr17:56468440-56469380 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxq1 | MA0040.1 | chr17:56468647-56468658 | CATTGTTTATT | + | 6.02 | | Nr5a2 | MA0505.1 | chr17:56469249-56469264 | AGGGTCAAGGTCAGT | + | 6.28 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_23473 | chr17:56468644-56469473 | Colon_Crypt_1 | | SE_28098 | chr17:56467989-56469859 | Fetal_Intestine | | SE_28995 | chr17:56467036-56469777 | Fetal_Intestine_Large | | SE_34462 | chr17:56468008-56470683 | HCT-116 | | SE_50030 | chr17:56465036-56470585 | RPMI-8402 | | SE_52476 | chr17:56468328-56469588 | Small_Intestine | | SE_56729 | chr17:56467057-56469075 | VACO_400 | | SE_56729 | chr17:56469101-56469831 | VACO_400 | | SE_57429 | chr17:56468222-56468962 | VACO_503 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 56468859 | 56469318 | | chr17 | 56468498 | 56468577 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I058389 | chr17 | 56467177 | 56469723 |
|
Enhancer Sequence | CCCAGCATTG TGCCTTGCAC CAGGGTTTAG TAATACTGAG TAATTGTGAA GCCAACCGGA 60
GATATGGAGT ACACTGAGGA CCAAACTTAG AAAGATTGTG AAGCAGTGGG ACAAATAAAA 120
AGGGTGAGGG ATGAGCCTTC AGACATGAGT GTGTGCTGGA AAATTGAGCT GAAAAATTAA 180
ATTTCTAATT CCAGATAATT CCTTTGCCAT TGTTTATTCC TGGTCAGGGA TCCCACCTCT 240
CCACCACTAC CCCCATTCCA CACCGCCCAA CACATTTTTT TCCTTCCAGC ATCAGCCAGG 300
TGCAGAACAA AAGGAAATTA ACGATTTAGT TATTGCTCCA ATGCTGAAAG TTTGAAAGTC 360
AGTCATTTGG AGCAGGTTCC ATTGTGTGTC CCTGCATGTC TTGGGCTTTG GTGGCTGTGC 420
ACAGAGTACC ATGGCTCCAG TCACCACAGT GGGGGCCAAC GCTGGACGCC CTGGCTTCTG 480
AGCAAGAGAG ATGAAAGGCT TCTTCTAATG TAATAACTGA CGGCCTCTCA GTGTCGTTTG 540
AACTGTTTAC AGGCTGAGTT AACGATTACA GGCAATGTGT ATCTTGGCCA GGTGCCCGAA 600
ATTCTTACCC ACCCGTCAGA TATTATCAAA GAGCCCTTCC ATGCCTGGCT GGAGTCCTTC 660
CAAAGCACCT CATAGAGATG CCGACACAAA AGGAGGAGTG TTCAGAATGT GCTCTCTGTC 720
TCTCCAGAGG CCAAGCAAGA AAGTCAGAGG ATCAGCATGA ATTAGGTGCT GGGGACACTG 780
AGTTTCCAGG ACCACTCAGG ACTGGGGAGA GGGTCAAGGT CAGTACTGGG GCCAGGAGAA 840
CCAGATTCCT TTTGAAGCAG TTTAGGAGGT GTATGTAAGA GTCTTTGCAG CTGGTAGCTA 900
AAGGATGGGG GTAGAAAAAC GACCCTCAAG ATGAAACAGA 940
|
