| Tag | Content |
|---|
EnhancerAtlas ID | HS184-14528 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr18:10725790-10727230 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr18:10727036-10727056 | TCTTGGGGGGTGTTGGGAGG | - | 6.1 | | RREB1 | MA0073.1 | chr18:10726124-10726144 | GGGTGTAGGGTGGTGGGGGG | - | 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 |
| GH18I010726 | chr18 | 10726399 | 10726663 |
|
Enhancer Sequence | GCCAACCACC ACGCGGGCCC TCCAGGGTGG ATGGAAGGCC AGATCCTGGG AATGGACTTG 60
GCTTGAGGAC ACACGGCGCC TGGTTTAGGA GGCGACTGGC CAGGCTGGGC AGGAGGGTGC 120
AGGGCACTAA CCACTATTTC TATCTGTCTG TCCCTCTTCA TCGAGAATCC TGTTGCTCTG 180
GGCAAGAGGT GGTTTTTACC GAAGGCATCA GCGTGACTGT TCAGAATAAT ATGGGCACCC 240
AGGATGTTGG GCAGGGTGGT ATATGTATTC TTGTGTCCAG GAGGGCTGGG GGCAATGTCA 300
GTTCGGGAGA GTTCGTGCAC GTGTGTGGGT GCGTGGGTGT AGGGTGGTGG GGGGATGGGT 360
GGGAGAGGAT TCATATATGT GAGCAACTGT GGATCCTTGG GTGCGAGTCC ACCGGAGGAG 420
GGGCTTCACG CTGCCTGGGG CTGGAAGAGC TTGTGTGCGA GCCTGTGTTC GGGAGCATGA 480
GAATGGAAGC GTCGCGGCCA GAGCCCCGGC CAGGTGGAGC AGGTGGGTCC CCGAACGCCC 540
CGCCCAGCGC TGCCTCCCTT CGCCTTCCCC GCAGGCACCC ACTACCTGCG GGGCGGTAAC 600
AACGCGCGCC AGCCGTGGCA CAACGCGGAG GGCCGGCTGC GGTACGGGCT ACGGCCGGCG 660
AACCCCACGA GGAGGGCCTG GCCACCCTGC ACAGCGTGCT GCTCCGCAAG CAGCCGTTCC 720
TGTGGCGCGC TGCGCTGCTC TGCTCTGCTA CACCAGCCGC CACGCTGTGC GTCTGTCCTT 780
CCGCCAGCTC TTCCAGGACC TGGCGCGCTA CGTGCGGGAC GCCGACGTGC GCTGGGAGTA 840
CTGCGCGCGC GCCAAGCGCG GCCAGACAGA CACCTCGCTG CCAAGTTAAT TCAGCAAGGA 900
CCAGGTGTAC CTGAACGGCA TCCTGTGCAT TCTGGGACAT CGCCAGACCA TCGATTTCCC 960
GCTGCTGACC TCACTGGGCA AGGTGTCCTA TGAGGATGTG GACCACCTGC GGCCCCATGG 1020
GGTGCTGGAT AATACCCGGA TGCCCCACCT TATGCAGGAC TTGGCACGCT ACCGGCAGCA 1080
GCTGAAGCAC ATCATGGCCA CCAACCGGCT GGATGTGGCG GAGCTGGGTC GCCTGCTGCC 1140
CGACTGATGT AGGTTGAGGG CTGCAGACAG AGGCCCTGGA CAGAAGCTCC AGATAGGCCC 1200
CCAGAACATG AAGCTGTTTG CTCTGTGCTT CCACGGTCTG GGTGTTTCTT GGGGGGTGTT 1260
GGGAGGGCAG GAGCATTCCT TGAGAAGGAG TGGCAACATC AAAGGGTTTG TGTCCCTTGC 1320
TAGCCTCCCT GGGGCCTGGG GATCTGCAGC AGCATGTCTG GCAAACTGAG TCGCCCTCCT 1380
GCCTCCAGCT CTGTGTTGAG CAGAGGGAAG GCATGGGGGC AGGAAGGGAG CTGAGCATTG 1440
|
