| Tag | Content |
|---|
EnhancerAtlas ID | HS133-08285 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr12:132356160-132357730 |
Target genes | |
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 | AAAAAAACCA AAAAAACCCA GTGGTTGTGC TACCAAGGTA TCCTTTTTTG GATGATGCCT 60
GGGGAGGATC AGTGAAGGAA ATACTACATT TCTGCTGGAG GTTAGCAAAA AGGAAGAGGT 120
GACCCCCCAG GCACGTTCAC AGGCACCCAG TGGCCAACCT TGCAGCCAAC CTTGGTCCAT 180
GGACCCCTGG TGTCAGCACT TGACTAGGGG GCATCAGGGA GAGCCTTGAG AGGGCGTGTT 240
CTCCAGTGGC AAAGAGCCTG TCAGTGCAAA GGCCCCGCGG CTGCCAGGTG CAGGGGATGG 300
GGAGGAAAGA AGGGGCTGCC CCCATTAGGG GTCTGGGGTT GGTGCAGGTC AGAGATGACA 360
GGGGCTCAGA CGCAGTGATC GGGGGATGGA GACAGGAGGG CAGGACTAGG GAAGGGAGGT 420
GAAGGAGATG GACATTTGGG CTGGATGTTG GGGAGGAGGG AGGGCGTGAG CTCAGGAGAC 480
TCACCTGGGT GTTGGGCCTT GGGTAGAACT GCACCATTTA CAGAGATGGG CAGATTCGGG 540
GAGGGCAGGT TTGCCCGCCT ACTTGGTGGA ACCAGGGCAT TGAGGATGTT GGAGGATTCC 600
ACGTTGGAGA GCAGAGGCGT GGGGAGCAGG AGCCTGCCCC GGCCCTGACT CAGCCCTGCA 660
AGGATTCTCC TGCCTGTGGC GGCTCTGCCT GCCTTCCAGA CGTGCTGTGA GGCTGGTGAC 720
CTGTCTGTCC CATCATGGGG CCGGCTACCG CTTGTGTCAG GCTGAGTCAC AGGCAAGCTG 780
CAAAGTCCCT GGGGCACTCT AAGGGCCTCT GCAGGAACCA GTCTGGCCGG CTGCAGGCTC 840
CTGGCCAGCT CGGGCCTCAT TGGGAGCTGC TGAAGTTCAA GGGCTGGAGC TCTCTGGGCT 900
GGGAAGATGC TGGATAAAGC TTGGGTCCCT GGCCCTAGCA GTTCCTGTCT CCCACTGTCT 960
TCAGGCCACA CTGGCCACAG CTCCCAGCCT CCTCCGTCCC ACCCTCACCC GGGCCTGGTG 1020
GAGAGGCTGG CGGGACTCCC ACACTACCGG GCAATGGTGT TCAGGAAAAG TGACTTTAGC 1080
AAAAGCTTCC TATGCACCCT TTGTGCTCTT GTCCTCCCCT TTCCCTTCTT CCCCCTCCTC 1140
ACGTCCTTTT TTATTTCAGT GAGACTCACA TGACACAAAA TCAAACATTA TGAAGTGCAC 1200
AACACAGCCG CAGTGCACAG TGCTGTGCAA CCACCTCCTT ACGCCAGCTC CGAAACGTTT 1260
CATCACCCAA AAGGATATTG CACACCCATT CGCAGTCACT CCTTAAGCGC TGCCCCCCAG 1320
GCCCTGACAA CCACTTTATT TTAATTTTCA TTATTACTTT TTTAGACAGG GCCTCACTTT 1380
TTTTCCCAAG CTGGAGCACA GTGGTGCAGG CATGGCTCAC TGCAGGCTCA AACTCCTGAG 1440
CTCAAGCGAT CCTCCTGCCT TGGCCTCCCA AAGTGCAGGG ATCACAGGCA TGCGCCACTG 1500
CACCCGGCCT CACTTCCTAT CTCTGTGGAT TTGCCTGTTC TGGGCATCTC ATATAAGTGG 1560
TGTCATACGT 1570
|
