| Tag | Content |
|---|
EnhancerAtlas ID | HS184-20217 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr3:43255960-43256810 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR1 | MA0112.3 | chr3:43256257-43256274 | TATGTCACAGTGACCTT | - | 6.28 | | ESR1 | MA0112.3 | chr3:43256257-43256274 | TATGTCACAGTGACCTT | + | 6.93 | | ESR2 | MA0258.2 | chr3:43256258-43256273 | ATGTCACAGTGACCT | - | 6.04 | | IRF1 | MA0050.2 | chr3:43256188-43256209 | TGAGTGTTTCATTTTCTCTTT | + | 6.13 | | PPARG | MA0066.1 | chr3:43256255-43256275 | TGTATGTCACAGTGACCTTC | - | 6.61 | | PPARG | MA0066.1 | chr3:43256256-43256276 | GTATGTCACAGTGACCTTCT | + | 6.74 |
|
| | 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 |
| GH03I043213 | chr3 | 43254556 | 43257984 |
|
Enhancer Sequence | GAAATAAATA AAAACACTAG TAGGTAGTAT AGGACTTTTT CAATGCTTTC TACATTTTCC 60
TATTTTTCTA CGATTGACAT ACATCCCCTT TCATGATGAA AAAGTTATAA AAATGAAAAC 120
ACGCACACAC AAATGTGACT TCCCCCTGGG TGTAAGGAAC TCCTTTATCT CATTCTCCCT 180
TCAGACAGCT GCCTCCTCAT CCAGCCCTGG TGAATCCCTC ACTTTGTCTG AGTGTTTCAT 240
TTTCTCTTTG CGAAATGGGC ACAATAATCC TGGCCTCTCT ACCGCCTAAG ACAGTTGTAT 300
GTCACAGTGA CCTTCTGCTA ATAAAACTCC AGGTAAACAC TAATTACCGT TGCTACTAAC 360
ACACTAATGC TTTCTGGGAG TGGTGAGTCA CACTAGGCTC TCATAAGGAA GGAATGGTCT 420
CCGGGGACAG GATTTGACAT GAAGACTCCT CTTGCCAGAA GACTTCTGCC TGTATAGATA 480
TCCAAGAGAG ACTGGAAGGT AGAGTGGTGT CTCCATCAGC TATTACTGAG CACCAAACAA 540
CCCAAAACCT CAGTAGCATA CCCCTGAGCA TTTGTTACTT GCTCACACAT CACAGATCAG 600
TGGGTATTTG GCTGATCTTG GCTTGGATCA GCAGGGTTGT GCCCCAGGCT GCAGTTTGGT 660
CCAGATCTGT TCCACATGCT TGTCATCCTC CGAGGACCAG CAAGCTAGCT GGGGCATGCT 720
CTTCTCATGG CAATGGCAGA GGTAGAAGAG GACACACACA GTCCCACAAG CACATTTCAA 780
CCCCTCTGTG CGTCACTTCT GCTAATATTC CATGGTCAAG CCCAAAGTCA AAGGGTGGGG 840
AAGTATTCTT 850
|
