| Tag | Content |
|---|
EnhancerAtlas ID | HS003-12290 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr12:132356180-132357550 |
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 | GTGGTTGTGC TACCAAGGTA TCCTTTTTTG GATGATGCCT GGGGAGGATC AGTGAAGGAA 60
ATACTACATT TCTGCTGGAG GTTAGCAAAA AGGAAGAGGT GACCCCCCAG GCACGTTCAC 120
AGGCACCCAG TGGCCAACCT TGCAGCCAAC CTTGGTCCAT GGACCCCTGG TGTCAGCACT 180
TGACTAGGGG GCATCAGGGA GAGCCTTGAG AGGGCGTGTT CTCCAGTGGC AAAGAGCCTG 240
TCAGTGCAAA GGCCCCGCGG CTGCCAGGTG CAGGGGATGG GGAGGAAAGA AGGGGCTGCC 300
CCCATTAGGG GTCTGGGGTT GGTGCAGGTC AGAGATGACA GGGGCTCAGA CGCAGTGATC 360
GGGGGATGGA GACAGGAGGG CAGGACTAGG GAAGGGAGGT GAAGGAGATG GACATTTGGG 420
CTGGATGTTG GGGAGGAGGG AGGGCGTGAG CTCAGGAGAC TCACCTGGGT GTTGGGCCTT 480
GGGTAGAACT GCACCATTTA CAGAGATGGG CAGATTCGGG GAGGGCAGGT TTGCCCGCCT 540
ACTTGGTGGA ACCAGGGCAT TGAGGATGTT GGAGGATTCC ACGTTGGAGA GCAGAGGCGT 600
GGGGAGCAGG AGCCTGCCCC GGCCCTGACT CAGCCCTGCA AGGATTCTCC TGCCTGTGGC 660
GGCTCTGCCT GCCTTCCAGA CGTGCTGTGA GGCTGGTGAC CTGTCTGTCC CATCATGGGG 720
CCGGCTACCG CTTGTGTCAG GCTGAGTCAC AGGCAAGCTG CAAAGTCCCT GGGGCACTCT 780
AAGGGCCTCT GCAGGAACCA GTCTGGCCGG CTGCAGGCTC CTGGCCAGCT CGGGCCTCAT 840
TGGGAGCTGC TGAAGTTCAA GGGCTGGAGC TCTCTGGGCT GGGAAGATGC TGGATAAAGC 900
TTGGGTCCCT GGCCCTAGCA GTTCCTGTCT CCCACTGTCT TCAGGCCACA CTGGCCACAG 960
CTCCCAGCCT CCTCCGTCCC ACCCTCACCC GGGCCTGGTG GAGAGGCTGG CGGGACTCCC 1020
ACACTACCGG GCAATGGTGT TCAGGAAAAG TGACTTTAGC AAAAGCTTCC TATGCACCCT 1080
TTGTGCTCTT GTCCTCCCCT TTCCCTTCTT CCCCCTCCTC ACGTCCTTTT TTATTTCAGT 1140
GAGACTCACA TGACACAAAA TCAAACATTA TGAAGTGCAC AACACAGCCG CAGTGCACAG 1200
TGCTGTGCAA CCACCTCCTT ACGCCAGCTC CGAAACGTTT CATCACCCAA AAGGATATTG 1260
CACACCCATT CGCAGTCACT CCTTAAGCGC TGCCCCCCAG GCCCTGACAA CCACTTTATT 1320
TTAATTTTCA TTATTACTTT TTTAGACAGG GCCTCACTTT TTTTCCCAAG 1370
|
