| Tag | Content |
|---|
EnhancerAtlas ID | HS095-08072 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr12:132356210-132357530 |
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 | GATGATGCCT GGGGAGGATC AGTGAAGGAA ATACTACATT TCTGCTGGAG GTTAGCAAAA 60
AGGAAGAGGT GACCCCCCAG GCACGTTCAC AGGCACCCAG TGGCCAACCT TGCAGCCAAC 120
CTTGGTCCAT GGACCCCTGG TGTCAGCACT TGACTAGGGG GCATCAGGGA GAGCCTTGAG 180
AGGGCGTGTT CTCCAGTGGC AAAGAGCCTG TCAGTGCAAA GGCCCCGCGG CTGCCAGGTG 240
CAGGGGATGG GGAGGAAAGA AGGGGCTGCC CCCATTAGGG GTCTGGGGTT GGTGCAGGTC 300
AGAGATGACA GGGGCTCAGA CGCAGTGATC GGGGGATGGA GACAGGAGGG CAGGACTAGG 360
GAAGGGAGGT GAAGGAGATG GACATTTGGG CTGGATGTTG GGGAGGAGGG AGGGCGTGAG 420
CTCAGGAGAC TCACCTGGGT GTTGGGCCTT GGGTAGAACT GCACCATTTA CAGAGATGGG 480
CAGATTCGGG GAGGGCAGGT TTGCCCGCCT ACTTGGTGGA ACCAGGGCAT TGAGGATGTT 540
GGAGGATTCC ACGTTGGAGA GCAGAGGCGT GGGGAGCAGG AGCCTGCCCC GGCCCTGACT 600
CAGCCCTGCA AGGATTCTCC TGCCTGTGGC GGCTCTGCCT GCCTTCCAGA CGTGCTGTGA 660
GGCTGGTGAC CTGTCTGTCC CATCATGGGG CCGGCTACCG CTTGTGTCAG GCTGAGTCAC 720
AGGCAAGCTG CAAAGTCCCT GGGGCACTCT AAGGGCCTCT GCAGGAACCA GTCTGGCCGG 780
CTGCAGGCTC CTGGCCAGCT CGGGCCTCAT TGGGAGCTGC TGAAGTTCAA GGGCTGGAGC 840
TCTCTGGGCT GGGAAGATGC TGGATAAAGC TTGGGTCCCT GGCCCTAGCA GTTCCTGTCT 900
CCCACTGTCT TCAGGCCACA CTGGCCACAG CTCCCAGCCT CCTCCGTCCC ACCCTCACCC 960
GGGCCTGGTG GAGAGGCTGG CGGGACTCCC ACACTACCGG GCAATGGTGT TCAGGAAAAG 1020
TGACTTTAGC AAAAGCTTCC TATGCACCCT TTGTGCTCTT GTCCTCCCCT TTCCCTTCTT 1080
CCCCCTCCTC ACGTCCTTTT TTATTTCAGT GAGACTCACA TGACACAAAA TCAAACATTA 1140
TGAAGTGCAC AACACAGCCG CAGTGCACAG TGCTGTGCAA CCACCTCCTT ACGCCAGCTC 1200
CGAAACGTTT CATCACCCAA AAGGATATTG CACACCCATT CGCAGTCACT CCTTAAGCGC 1260
TGCCCCCCAG GCCCTGACAA CCACTTTATT TTAATTTTCA TTATTACTTT TTTAGACAGG 1320
|
