| Tag | Content |
|---|
EnhancerAtlas ID | HS184-08816 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr12:125367970-125368720 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr12:125367976-125367994 | GGAAAGAAGGAAAGCAGA | + | 6.17 | | EWSR1-FLI1 | MA0149.1 | chr12:125367972-125367990 | GGAAGGAAAGAAGGAAAG | + | 8.48 | | HSF1 | MA0486.2 | chr12:125368110-125368123 | GAATCTTCCAGAA | - | 6.09 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_27703 | chr12:125367887-125370962 | Fetal_Intestine | | SE_28633 | chr12:125367217-125371115 | Fetal_Intestine_Large |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I124883 | chr12 | 125367867 | 125370882 |
|
Enhancer Sequence | AAGGAAGGAA AGAAGGAAAG CAGATTCTGA GTTCTCACCC CAGACCTGTG ACTCAGACAC 60
TGGGGAGTAA GGCCCAGGAA TCTGCATTTT CACAAACCCT CCAGGGGCTT CTGACTCACT 120
CTGGAGTGAT GGGTGAAGTG GAATCTTCCA GAAGGACAAA TGCTTTCAGC CATGTCTGGT 180
GTCAGAGGCA GGAGCTCCCA CACTTATGTG CTGCCTGGCT CCTCACCAAG ACAGGTGCTA 240
GACTATCTCT GAGACTATCT TTTCCCTTGA GGCAGCTGAG AGCTGGAGCA GCTTCAGATG 300
CCTCCAGATC CTGGGCCCTT GAACTTCAAC TCGAACTTGG CTCTAAAGTG TCGCCCTCAG 360
CAAGAGTCAA CGCAATTGGG CCCTGGCTCC GTGAGGTGGA CAGGGGCCTT GCTCGCTCCT 420
TCTTCCCCAG CCCTGCCCCA TGGGGGAGAG AGAGAGGTCG TCAGGTGAGA CGGAGTTTGT 480
TTCAGCAATG TGTTTATGAG TCCCAAGAAC TTAGGATAAA GTTTCTGAAA TACTAGCCTG 540
AGGATGTCCC TCTTTGAGAA AAAGGGAAAA AGGACACCGC GGTTACCCCA GCTTTGTTAT 600
TCATGTAACA ACGGCAGGGC ATTTGAGTTC TTTCTGTTTT CATCCTACTT CCACTCCCAC 660
ATCTAATCAC TAACATTTCT CTTGTTTTGC TGTTTGTTGC TTCCTTTCAT TCTCCCCATC 720
TGAGGTGGGT AGAATTGTGT CCCTCCAAAA 750
|
