Tag | Content |
---|
EnhancerAtlas ID | HS133-03428 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:209978550-209979290 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr1:209978709-209978729 | CCCCAGAGCAACCACACCCC | + | 6.16 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_27309 | chr1:209977673-209980487 | Esophagus | SE_27823 | chr1:209977468-209983975 | Fetal_Intestine | SE_35823 | chr1:209974126-209984775 | HMEC | SE_64223 | chr1:209974556-209984573 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 209978699 | 209978810 | chr1 | 209979142 | 209979287 |
|
Enhancer Sequence | CATCCACCAA GAGAACAGGT TGGAACAGGA TGACCCCTTT ACCACAAAGC AGGCTCCCTG 60 TAAAGAGTGA CACCTCAGGC CTCCTTTCCA AGTCAGGCCT GGGAGACTTT CCCCATTCTC 120 CACACCACCC TCCAGCCCCT TCGGGCAAAG AGGGCCCACC CCCAGAGCAA CCACACCCCA 180 GCGCCACCCT CCCCAGCACC TAGCTCCGCT CCTTGGAAAT CCAAGGTTGT CTCCCAGGCC 240 CAGGGCGAAG GGCCTAACTG TGCCAAACAG ACTCAGGGAG GGAAGACAAA CCGCCAATGC 300 TCCAAAGCTC CTGGCCACCC TCACTCCAGT TTCCCAAAAC GCCCACTAGG ATCAAGGACC 360 TGCGGACCTG GGAAGTCCCC TCTCTGGGAC ACAGGGGCCA GCCGCAAGTT GGTAAGACTG 420 AAGGGGGCGC GGTGCTTTAG CTCTACCGGA TAGTGGGGTT GTTGACGGCC GAGAGCAGTG 480 CCCTCCGCTT CGGCGGTGGG GGTAGGGAGA GTAGACACAA GTGTAGATTC GAGAGGGGCC 540 TAGCGCTACA GAACTGAGGC CGCCCCAAAG CTATCTGGAA AAGGGCGACA GGCACCCAGC 600 CCCAGTGGGT ACCCACCCCA AACACACAGA TGCCCCCAAG CAAGTTCTCT CACCCCCTAC 660 AAACTCCGGG GATGGGTCCT ACCCCACCCA CGGGGGAGCC TCTCCTCCCT CAAGCTGGTC 720 CCCAGAAGTT GGCGTACCCA 740
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