| Tag | Content |
|---|
EnhancerAtlas ID | HS184-08877 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr13:20694510-20695140 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr13:20694545-20694563 | GGAAAGAAGGAAGCAACA | + | 6.13 | | EWSR1-FLI1 | MA0149.1 | chr13:20694541-20694559 | GCAAGGAAAGAAGGAAGC | + | 6.8 | | NFYA | MA0060.3 | chr13:20694854-20694865 | GACCAATCAGA | + | 6.14 | | NFYA | MA0060.3 | chr13:20694905-20694916 | TCTGATTGGCT | - | 6.32 | | NFYB | MA0502.1 | chr13:20694849-20694864 | GAAGCGACCAATCAG | + | 6.36 |
|
| | 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 |
| GH13I020118 | chr13 | 20692140 | 20695980 |
|
Enhancer Sequence | AGCAAAGAAT TGAACAAAAC GCACAAACAA AGCAAGGAAA GAAGGAAGCA ACAAAAGGAG 60
AGATTTATCG AAAATGAAAG TACGCTCCAC AGGGTGGGAG CCGCTGGAGC ATAGGGGCTC 120
TTTTTACAGA ATTTTCTGGG GTTTAAATAC CTTCTAGAGG TTTCCCATTG GTTACCTGGT 180
GTACACTCTA TGTAAATGAA GTAGTGACCT GCAACCAGAG GCTGAGGTGA AGTTACAAAG 240
GTTACACCCG ATGCAAGCCT CTGTTTGCAA AGTGAAGTTA CAAAGTTACA GTTCTATGCA 300
AAGGAAGACT TGGCCCACAA TCAAGCTGAT TGGTTGTGGG AAGCGACCAA TCAGAGGCTG 360
AAGTGAAGTT ACAAAGTTAC AATCCTATGT AAACGTCTGA TTGGCTGCCC TCAGAGACAC 420
TTTCAATTTT CCATCTGCCA GGCAGAAAAG GGTGGGGGTT TGCAAAGGGA GTAGCCTCCG 480
GTTTTTTGTT TGTTTTTTCT TTTTTGAGAC GGAGTTTCAC TCTTGTCGCT CAGGCTACAG 540
TGCAACGGCG CGATCTCCGC TCACTGCAAC CTACGCCGCC CGGGTTCAAG CGATTCTCCT 600
GCCTCAGTCT CCCGAGTAGC TGGGGTTACA 630
|
