| Tag | Content |
|---|
EnhancerAtlas ID | HS184-04508 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr10:99436390-99437180 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr10:99436598-99436617 | TGGCCACCAGAGGGCAGCC | + | 8.2 | | Foxq1 | MA0040.1 | chr10:99436537-99436548 | AATAAACAATA | - | 6.62 | | ZNF263 | MA0528.1 | chr10:99436941-99436962 | TCTTCCCCCTTCTCCTGATCC | - | 6.6 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_28147 | chr10:99436427-99438003 | Fetal_Intestine | | SE_28882 | chr10:99433970-99438167 | Fetal_Intestine_Large |
|
| | 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 |
| GH10I097676 | chr10 | 99436061 | 99437105 |
|
Enhancer Sequence | CCTGTAATCC CAGCTACTTG GGAGGCTGAG GCAGGAGAAT CACTTGAACC CGGGAGTTGG 60
AGGTTGCACT GAGCCGAGAT TGCACCACTG CATTCCAGCC TGGAGTAAGA CTTTGTCTCT 120
CAGTAAATAA AAATAAATAA ATAAATAAAT AAACAATAAA ATAAAAAAGA GGACCTACCT 180
GACTCAAGGT AGTAGTGGTT CCTCCTCTTG GCCACCAGAG GGCAGCCCTG CCCTGTGTAC 240
ATCACTGCCC CACTTCAAAC CCTGAATAAT CAAGCATATA GGGTGGGTGG AGAGGGAGAA 300
GAAAGCTAAT AAGCACAGAG TATGCCTCTC TTGAGGTGGA GCCAGAACTG TGGGAAAAAC 360
CCTGCCTTCA AGGGTTTCCA GGCCATGGGA AGCCTAGGAT ATAACGCAGG CAACTTCAGA 420
ATCATCAGTC CACCTTGGGA TGGTCAGCCC ATAAGGATGA AGAAACCAAA TGAGGATCTG 480
GCACCACTAG TTTGACTACA GATTAAGCCA GCCCAAGGCC TCAGCCTACT GTGCTGGGCT 540
GACCATGACA GTCTTCCCCC TTCTCCTGAT CCTATGGATC AGGACTGCTG CAGAGACTCC 600
CCTCTTTACT CCCGATCCAA CAGACTCTGG AAAAGGAGGC TGTGGTCCAG GGGCTCAGCA 660
TGGGGGTGAA AAAGGAGAGG GAGGTGAAAA GGAGAGAGGA GGCCAGCCCT GATTTTTCCT 720
TCCTGGGGAC ACTCTTGCCC CTCCCACTCT GTTTCATTTC CTCCCCTTCT GTGACAGACT 780
CACACAGCTC 790
|
