| Tag | Content |
|---|
EnhancerAtlas ID | HS184-03212 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr10:5580460-5581200 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOXF2 | MA0030.1 | chr10:5581032-5581046 | TCACCGTAAACAAG | + | 6 | | TCF7L2 | MA0523.1 | chr10:5580610-5580624 | TGTCTTTGATCTTG | - | 6.03 | | TP53 | MA0106.3 | chr10:5581040-5581058 | AACAAGCAGGGGCATGTA | - | 6.1 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_26546 | chr10:5580389-5581430 | Esophagus | | SE_33798 | chr10:5580365-5581432 | HCC1954 | | SE_35816 | chr10:5579269-5582288 | HMEC |
|
| | 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 |
| GH10I005536 | chr10 | 5578510 | 5583878 |
|
Enhancer Sequence | CACGCGTGAG CCACCGTGCC CGGCCTGTTT CTTCTACTCC TGACCCTCTC TCCCCATCTT 60
TGCTCGGTAC CGCCACTTCT TTCCAAATAC AACCCAACTT CCACTCTGGC CTAACATATT 120
TTTCCCTGGT ACTCATTCAT TGTTTAAGAA TGTCTTTGAT CTTGGGACAC AGCCTTAATG 180
CAAGTTGTTT TTCCTTCCTG TGGTAAGAAA GCTTCAGGAG CCTTTTCCCT TCAGGCTGCA 240
GAACTGGGAG CAAGCACAGC TGATGCCAGC TCCTCCTGCT CCTGTTTTCA CAGGTCCTGC 300
CCTCCAGGGG AATGTTCCAG GTACATTCTG CGTCTCAGAG ATAATGCAAA AGCCAAAGAG 360
ACAAGCACAA GTCAGTTATT TGGGGACCCC TCTAACTGTG TTTTCTTTAG TTCCATCTGT 420
TTCTGTCTGA CTTTCTACAG AAACCTACAC CCTGTATGCT TTATCACTCA GGGAATAAGT 480
TCTGCTGGAA CGTCCTCGAT GAGCTATGCA TAGCAAAGTT AAGTCTTGTT CCTCAAATAG 540
CTCATTCTCC AGGATCTGTG GACACAAAAC AATCACCGTA AACAAGCAGG GGCATGTAAG 600
CAACCAGACG CACAATGCTG ACCACAGAGG CGCCTGGTCT GAGAAGGGAG AGCCCAGGGC 660
AAGCCGGAGG AATCACCGAC ACCTTGCAGG AGAGGAGGGG AGAGGAGGGC TGGGCTGCGC 720
TTGAAGGGAG GAGGGTGCCG 740
|
