| Tag | Content |
|---|
EnhancerAtlas ID | HS184-17254 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr2:208693220-208694120 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr2:208693921-208693932 | GGATGACTCAT | + | 6.62 | | JUN(var.2) | MA0489.1 | chr2:208693346-208693360 | GGGAGATGACTCAC | + | 6.02 | | JUNB | MA0490.1 | chr2:208693921-208693932 | GGATGACTCAT | + | 6.62 | | Rhox11 | MA0629.1 | chr2:208693977-208693994 | TGTTTTTACAGCGAAGT | - | 6.08 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_23192 | chr2:208692923-208693828 | Colon_Crypt_1 | | SE_28346 | chr2:208693094-208693987 | Fetal_Intestine | | SE_32146 | chr2:208693054-208693856 | Gastric |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 208693538 | 208693694 | | chr2 | 208693862 | 208693970 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I207828 | chr2 | 208692781 | 208698619 |
|
Enhancer Sequence | CTGCAAAAGT CAACCATGGA TATGATGAGC AAGACTGAAG CCAGCAAGAC ACAAATGGGA 60
AGCCCTGTGG CCTCAGGTGC AGCTGGTGGC ACAATCTACT GTTCTGGACA ACCCTGCCAA 120
TGGGAAGGGA GATGACTCAC TGAAATGAAC TGTTTGTTTT TCCAAAATGC TCAAGGTTGA 180
ATTTCACTTG AAAAACATTT TTGCTTTTCT GATCTGAACT AGGGCTTATG AGTGGGGGGG 240
AGTCCGCAGT CACCCAGCAA TTCTGGTTAT AGTGACAATG GACAGAACAC CAGAAGCTCT 300
CCATTGAGAA GGGAATTGGC AGTGACTCTA GAGTGAAATG ACAGAAAATG AGAGGGGAGT 360
GCCTCGTGAA AACGCTCGGC ACACCAGTGA CAGCCACAGC GTTACATCCA TGGCGAGGCA 420
GCTTTCTACA TCAGTTAACA CGAGCTAAGT GGTTCTCTGT TAACTAGCTG CCTTTATTTG 480
ACAGTTTGAA AAGATAAAAT GACACATTTT CATTTTCTGA ATGACATCCT GTGGTCTATG 540
AAATCTTGTG AGTTTTTTAA AAATTAGGAA AAAACTCCTA CCTTTGTAAG TCTACCTTTA 600
TAACATGAGC GTGAACATTA AAGCAGGAGA CAGTGGGGAA GAAAACATTT TTCAAACAAT 660
ATGACAGATA TTGTAATATG TAGAGAGCAA ACATTCCAGG TGGATGACTC ATTTGTTGTT 720
TGGCTTGGTG GAAGCCTGCA CGGGAGTCTA AATAACTTGT TTTTACAGCG AAGTTTTTAT 780
TTATTTATTT TTTTGGAGAT AGGGTCTCAC TCTGTCACCC AGGCTGAAGT GCAGTGGTGT 840
GACCTCGGCT CACTGCACCC TCTGCCTCCT CCTGGGCTCA AGTGATCCTC CCACCTCAGC 900
|
