| Tag | Content |
|---|
EnhancerAtlas ID | HS184-08855 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr12:132356220-132357540 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr12:132357274-132357295 | TCCCCTTTCCCTTCTTCCCCC | - | 7.17 | | ZNF263 | MA0528.1 | chr12:132357280-132357301 | TTCCCTTCTTCCCCCTCCTCA | - | 7.41 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_43473 | chr12:132356077-132357785 | MCF-7 |
|
| | 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 |
| GH12I131871 | chr12 | 132355750 | 132358503 |
|
Enhancer Sequence | GGGGAGGATC AGTGAAGGAA ATACTACATT TCTGCTGGAG GTTAGCAAAA AGGAAGAGGT 60
GACCCCCCAG GCACGTTCAC AGGCACCCAG TGGCCAACCT TGCAGCCAAC CTTGGTCCAT 120
GGACCCCTGG TGTCAGCACT TGACTAGGGG GCATCAGGGA GAGCCTTGAG AGGGCGTGTT 180
CTCCAGTGGC AAAGAGCCTG TCAGTGCAAA GGCCCCGCGG CTGCCAGGTG CAGGGGATGG 240
GGAGGAAAGA AGGGGCTGCC CCCATTAGGG GTCTGGGGTT GGTGCAGGTC AGAGATGACA 300
GGGGCTCAGA CGCAGTGATC GGGGGATGGA GACAGGAGGG CAGGACTAGG GAAGGGAGGT 360
GAAGGAGATG GACATTTGGG CTGGATGTTG GGGAGGAGGG AGGGCGTGAG CTCAGGAGAC 420
TCACCTGGGT GTTGGGCCTT GGGTAGAACT GCACCATTTA CAGAGATGGG CAGATTCGGG 480
GAGGGCAGGT TTGCCCGCCT ACTTGGTGGA ACCAGGGCAT TGAGGATGTT GGAGGATTCC 540
ACGTTGGAGA GCAGAGGCGT GGGGAGCAGG AGCCTGCCCC GGCCCTGACT CAGCCCTGCA 600
AGGATTCTCC TGCCTGTGGC GGCTCTGCCT GCCTTCCAGA CGTGCTGTGA GGCTGGTGAC 660
CTGTCTGTCC CATCATGGGG CCGGCTACCG CTTGTGTCAG GCTGAGTCAC AGGCAAGCTG 720
CAAAGTCCCT GGGGCACTCT AAGGGCCTCT GCAGGAACCA GTCTGGCCGG CTGCAGGCTC 780
CTGGCCAGCT CGGGCCTCAT TGGGAGCTGC TGAAGTTCAA GGGCTGGAGC TCTCTGGGCT 840
GGGAAGATGC TGGATAAAGC TTGGGTCCCT GGCCCTAGCA GTTCCTGTCT CCCACTGTCT 900
TCAGGCCACA CTGGCCACAG CTCCCAGCCT CCTCCGTCCC ACCCTCACCC GGGCCTGGTG 960
GAGAGGCTGG CGGGACTCCC ACACTACCGG GCAATGGTGT TCAGGAAAAG TGACTTTAGC 1020
AAAAGCTTCC TATGCACCCT TTGTGCTCTT GTCCTCCCCT TTCCCTTCTT CCCCCTCCTC 1080
ACGTCCTTTT TTATTTCAGT GAGACTCACA TGACACAAAA TCAAACATTA TGAAGTGCAC 1140
AACACAGCCG CAGTGCACAG TGCTGTGCAA CCACCTCCTT ACGCCAGCTC CGAAACGTTT 1200
CATCACCCAA AAGGATATTG CACACCCATT CGCAGTCACT CCTTAAGCGC TGCCCCCCAG 1260
GCCCTGACAA CCACTTTATT TTAATTTTCA TTATTACTTT TTTAGACAGG GCCTCACTTT 1320
|
