| Tag | Content |
|---|
EnhancerAtlas ID | HS129-03712 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr1:228224310-228225760 |
Target genes | | Number: 27 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr1:228225321-228225336 | CGACCCCTGACCCCC | - | 6.39 | | NR2F1 | MA0017.2 | chr1:228224448-228224461 | CTCTTGACCCCTG | - | 6.04 | | REL | MA0101.1 | chr1:228225575-228225585 | GGGGATTTCC | + | 6.02 | | Zfx | MA0146.2 | chr1:228224638-228224652 | GCGGGCGAGGCCTG | + | 6.65 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TCAACCTGCC TGGGGTAGAA AGCATTTGAG GAATTTTAAG TGCATGGAGA CTGGGCACAC 60
CGTGCAGCTT CTCTGTCCCC TGCCGCAGGA CCCAGGCACT GGGAGGGCTC ACTTCCCTGC 120
AGAGCTGGAG ACACCTCACT CTTGACCCCT GGCAAGGTAA AGCTGGCAAG GACACAGGTA 180
CAGAGAAAGG GCAGGGACGG CTGCAGTGGA TGCAGCAGCC CAGGGCCCAG CAGCTGGATC 240
TCAGGCAGCA CGTGGCTCTG CAGAGAGCCT GGCCTGCTCT AGGCCAGGTG GGGCATGTGC 300
TCCTTAGAGA AGGGGACAGA GGCCAGGAGC GGGCGAGGCC TGGAGCCTAG GGATGCCACC 360
TGTGCCCACA TGCTCGGTGC CCTCTAACAT GGGCTGGGCC CAGGAGTCCC CCCGGGCCCT 420
GGCACCTGCC AGATAGGTCG GGGGGAGTGG AGTGGCATGG GGAGGTATGC AATCTCTTGT 480
GCTTCCCAAG TAAGTGTGCT TCCCACAACT CCCAGTGGAC ACTTCCCAGA GCCCTGGGGT 540
TTGCTTCTTC GTACCCAGTG TGGGTGGGGC CTGCAGCAGT GGCCCTCCCA CTCAGCCTTC 600
ACACACCACC CCCTCTTCAA GCATTTCCAG TCCCCACCCC CTGCCCTATT CTGTGAACCC 660
CAGGGTATCC CCACTCAAAG CACACGGCCA GATTCCTGGT TGGTGCCCCA GGACCCCTCC 720
AGCCCCAAAG GGTGGGGAGA GTAATGAAAG GGTCCTGCGC ACCACATGTC AGTAAGCCTT 780
GTTGGGTGCC CCACAAGTCC CCCTTCATCT CTCCAACGTC TTCCCCAGGC AGGAGACAGC 840
CCAGCCTCCT CTCCTCCCCG CTGAGCCCCC AGGAGCCCCT CGGGGGTGGT CCGCCACCTC 900
CCTGTGTGTC CCCTGCCTAT GAGGGCCGGC ACAGGGGTGG GGCCTGCCTG CTAGGACATG 960
GGGACACACA GGGCAGCTCT TTAGGGAACC AGCGTCCCCA AAGCCAGGTT GCGACCCCTG 1020
ACCCCCCCCA TCGGAAAGTG TTGCCGTTTA AGATGCGTTG GGGTGGGGGG CTCCCCTGGC 1080
TCCAGCGGCC TCTCTGGTAT ATCATTAACT CTCCCCAGTG GGAGGGGAAC CCCGGCCGAC 1140
TCCCCGCCGC GTCCGGCTGG GAGCACAATA TCCCAGCGAC GGCGACAAGA TTAAGCACAA 1200
GGGGAGAGTG CAAATGCGCG GGCGGTTCAC ACGCCCTTCG CGGTGCTGAA TTAAAGCGTC 1260
TGAATGGGGA TTTCCCCTCG CGCCGGACGG CCTGGCGCGC GGCGCATACT TCCAGGTTGC 1320
TATGACTGGC CTGCGCTCGC CTAATCACCG ACTAGGGGGA AATTCATATA AAATATCGCC 1380
GGCCATTGTG GGCCTAACTC GGCGTGACAG TGGCGCACAA AGCCGGATTC AAGCGCCCCA 1440
GCGGGTCAGC 1450
|
