| Tag | Content |
|---|
EnhancerAtlas ID | HS184-06695 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr11:118560160-118561880 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr11:118560527-118560547 | CCCCCACCCCACCCACCCCC | + | 6.09 | | RREB1 | MA0073.1 | chr11:118560532-118560552 | ACCCCACCCACCCCCAGCCA | + | 7.54 | | RREB1 | MA0073.1 | chr11:118560528-118560548 | CCCCACCCCACCCACCCCCA | + | 8.4 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AAGTGCCGCC AAAGTGGGAG TCCAGGCAGA GGAGGCGCCA AAAGCGAGCA AGGGCTGTGA 60
GGACTGCCAG CACGCTGTCA CCTCTCAGTG GGGGCTGTGG GCTCTCTTCC CAGGGGCACT 120
GGCCCTGCCT AACCCTAGCG GTACAGGGAG CACCAGTCAG CTCCTCCTCC AGGCCCACAT 180
GCAGGTGAGC ACACTGAGGC CTGGGGCGGG GATCGTGGGC AGCAGAGCCC AGGAGTTTCC 240
TGTAGGGTGA TGGCCAGCCC ACCCCTGGCC TGCTCACCTG AACTTCATAC TCCCCTCCGC 300
CACCGGGCTC TCCACCGTTG CTAATGTCAT ACTGGGAATA AGAGGGCGGG CCGTAGGTCA 360
GGCACTGCCC CCACCCCACC CACCCCCAGC CACAGGGACA ACAAACAACG GGATCCTTGT 420
CGGGAGAAGC CGCTCTGCCT CCCAGCAGCC CCTGCAGTGC CCAGGAGTGC CCACTGGGCG 480
CCGCCACCAT CCCAGCTGCG CTTGCCCTGA GCCCTGCCAA GCCTGACCCT CCCGCCTCAC 540
CACGGGGACG CCCTGGGGGT ACGGGGAGGG CTCAGGCCAG CTCATCTTCT CATACATGGC 600
TGACTTGCTG GTAGACATCA AAGTTGGTTC GGATCCAATT CTGGGGCATA TTGGTAGATC 660
AGGATCTGGC TGCCCTAGAA GGTTCCAGAC ATTCCCGTGA CTGTGGGTGG GGCTGGACTG 720
GGAGCCAGGA CGCTGGGCCC GGCGGGAAGC CAGATGTCCC TTTCCTGGCC CTTCTCTTCT 780
CGGCTCACAG CTGCCCCCCG GTGGCTCCGC GGGACCTGCC GGCTGGGACA AGGGGCACAG 840
CCGGAGGAAG CGGCCTCCCC TGCAGGTCCT GCTCAGGGTC GGGAGGGGGC AGTGCTGCCT 900
GCAGTGGGCC AGAGCCACCT TCTGTGCCCT CACCTCCAGG TATTTCAGAG CCTTGTCCGC 960
CACGCCAGGG TCAGAGAAAC ACCCGTTCCA GAGTGGAGTG AGGTTGGATG GGTAAAACTC 1020
CCGGTTCTCC TTGTTCTCAA GGTCGTAGTC GAACCAGGCA CTGGTCTGCT CATCCCACAG 1080
GACTGTGTTC AGGGCGGCCA AGCGCTGCGC CGGCAGGATT CTGTACTTTG TGGCCTGGGA 1140
GTCGTTCCCT GGGGCAGTGC TGCCTTTGGG CCCTACAGGA GCCCTCTAGA AAGAACTTCT 1200
GAGGTCAGAC GGGCAGCATC TACTCTAACG CCTCACCTCC TCCAGGAAGT CTCCCCACCC 1260
TCCCCAGGAA ACCCCAGCCT GTCCTGTCTC CTCTGGGCTG CCTGCACTGT CTCTGGCACC 1320
ACTGGGTAGA TGTTCACTGC CTGCTGGGCT CTCCTTCCCT GAGCTCCTGG GCCAGGCCTC 1380
CGTCTCAGGA GGAATCAGGG CTACTGCTTG CTCAGCCCCG TCCTGAGCTA CTTTGCTCAT 1440
CCACATCCCC TCATCTGGGG AAAGGGTTTG GGGTTTTATC CCGTCCCTAG TCCTACCACT 1500
GGAGCCCAAG CCCAGACCCT CTTGCTTGGA GCCCCGCTTT CCCTGGACCT GTTCCCACTC 1560
TGCCCCAGTC ACACAGGCCT TCTTCCCAAT CCCTGAACAG TGCCTCAGGG CCTCTGCACG 1620
GCCCTTTCCG TGCCTGGACT GTCCTCTCCC AGATCAGCTC AGCAATGGTT CCTGCCACAA 1680
TTCTGCTCAC ACATCACCTC CTCAGAGACA CCTTCCCTCC 1720
|
