Tag | Content |
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EnhancerAtlas ID | HS133-03463 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:211816640-211817460 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
STAT3 | MA0144.2 | chr1:211817317-211817328 | CTTCTGGGAAG | + | 6.14 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_28267 | chr1:211815367-211818806 | Fetal_Intestine | SE_29189 | chr1:211815501-211818772 | Fetal_Intestine_Large | SE_34866 | chr1:211807990-211818745 | HeLa | SE_54270 | chr1:211815737-211817861 | Spleen |
|
| Number: 1 | ID | Chromosome | Start | End |
GH01I211641 | chr1 | 211814677 | 211818948 |
|
Enhancer Sequence | CAGGGTCTGA CCTGGAGTAA AAGCTCCATG AATGCCGGCT GTCCTGTGGC CTCCCCGACA 60 CGTCCCCCCT GCTGGAAGGC TTTCCTCACC ATCTCCCTCA TAAACAAAGC CAAGGTCAAG 120 GCTGCAGCCC ATGGTGAGAG CAGGGAGAGC TTGTGGGAAG TTCACTGCCC CGCCATGCCC 180 CTGAATGGTG AGCCTCTTTC TTTGATGTGG GCTAACATCC GTGGACTCAG AGGCCCAGAA 240 AGTGCGAGAC ACGCCAAGGC TCGGCCCCTG GGCGTCTGTT TCCTGAGCAG CCTGGGACAC 300 AGGTTGCCCT GGTGAGATGA CCCACAGTCA GCACCCTAGG CCTTGGCATT ATGCGGGCAG 360 CTGGTATGAG CCCTGCCTCA CCCTGCACAG AATTTGCCAG CTTCACAGCA TTCCTGCCAG 420 CCCAGCCTGC TCCCAGACCC AGCCAAGTTT CACTCAGGCA GCCTGCATTC CCATTTTGTG 480 CGCCTTGTCC TGCCCAGAGG CACCGGCTGC TGAGGGAAGC ATGAGGTCCT TGGAAAGGAG 540 CTGCCCCAGC AGGCCGGTGT GCTGGGAGCC CTCAGCCTCT TCTACACTCC CGCCACCCCC 600 AGCCCTGCAT CCTGCCCCAA GCTGGCTGCC TGCCAGCTTC TCGGGTCTCA TTTACTTACT 660 GCTGTTTGTT TTGGAGGCTT CTGGGAAGCA AGGCTCCACC TGAGGAATCT TTGGCTGAGG 720 GGACTTGTGA CACCTGAGAC TTTGAACTTT CAAGAAAACA TAAGGCTCCG CTGGCCACTT 780 CCCCGGGTGT GGGGACAAAT GTCACTGCAG TGCCGTGGGC 820
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