| Tag | Content |
|---|
EnhancerAtlas ID | HS184-07648 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr12:53272850-53274190 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr12:53273885-53273904 | TGCTGCCTCCTAGTGGATG | - | 6.09 | | RREB1 | MA0073.1 | chr12:53273591-53273611 | CCCCCCACCCACCCCCCACC | + | 6.39 | | RREB1 | MA0073.1 | chr12:53273592-53273612 | CCCCCACCCACCCCCCACCA | + | 9.3 |
|
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_23067 | chr12:53272391-53273900 | Colon_Crypt_1 | | SE_23945 | chr12:53272387-53273885 | Colon_Crypt_2 | | SE_26564 | chr12:53260695-53274096 | Esophagus | | SE_34862 | chr12:53272821-53274199 | HeLa | | SE_56286 | chr12:53272670-53274165 | u87 | | SE_57699 | chr12:53272845-53273859 | VACO_503 | | SE_64566 | chr12:53266900-53273597 | NHEK | | SE_65517 | chr12:53272588-53274254 | Pancreatic_islets | | SE_67099 | chr12:53263476-53274484 | H2171 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I052878 | chr12 | 53272285 | 53274184 |
|
Enhancer Sequence | AATCCTAACT AAATTGGGAA GATGAAAGGC TCACAAGTGG ATGGGTCAGC CATAGGAGGT 60
GCATTGCAGA CAGGGGGACA GCAGGCACAG GGGCTAAGGG TGTGAGGGGG TGCGACTTCC 120
TCAGGGAACC CCCAGGGGAT TCAGCTGCCT GAGTGGAAGG CCACGGCAGA GGTGACTTCA 180
GCGGGGTCAG GCGGGCCTGG AGTGCCAAGC TCAGGGGCTT GTGTGTCTCC AAGGAAGGGT 240
TTGGGCCAGG CTGGGACATG ATTGGGATCA ACTGGAAGGA GTGCTGTGGA GGAAGGCGCA 300
CTGAACTGAG AGTGAGGACA CGGAAGTTCT CACCCTGGCT CTGCCCGATG CTGCCCAACT 360
CCCCTCTCTG AGCCTCCAAA ACGACAGCGT GCTGCACCTC GGAGCCGCTG GCTCACAGGC 420
GGCTGCTTTC TCCTGGGGCC TGTCTGCTGC CGGCTTGCCT GTCCTCCTGG GTCCTGCCCA 480
CGCGCTTCTG CCCCCAGGCC CGTGCAGGCG TGGACCTCCC GCGAGGGCCT CAGCAGTCTC 540
CAGGACAGAG AGTGGAACCC GCCACCTGCT GGAAAGGCCG GAGCCGGCGC AGAGCTAGCG 600
CGGGGCAATG TGGCGCCCTC TGCGGGGAGC CCCTGCTGCC TCGCGCCGGC ACTCAAACCT 660
CCAGTACACA GTGCAGTGGA GGGCACACCA GCAGCAGCAC GCCTGTCTCA CCCTGCTCCT 720
CAGTGCCCTC CGCCCTCAGC TCCCCCCACC CACCCCCCAC CATGGCCCCT GCGTTGCCAA 780
GGGCACAGGG CATAGGAGGA CGTGGACTGA TCCACCCCAA GCTCCGCTCA CCAAGTCATG 840
CCCTAGCCTA CATTTCCCAT GAGGATGGGA GCTTCCTCTG ATTTGCACAA AGCCCCCCTG 900
TCGGTTAGTG GTGGCCTGCA ACCCAACAAC CTCCCAAGTC AGCCTCCTGG GATAGGGAGG 960
ATGTAGTGAG GGGGTGGGAG GGTGTGCAGG CTCGGCTTCC AGAAGCCGGG AGAGCAGTTT 1020
CTTTCCCTGC TCCTCTGCTG CCTCCTAGTG GATGTCTGAT GTCTCTCCGG TTTGCACAAA 1080
TCCATCCCGC TTCGGTCAAT CCTAGCCGTC TTGGTGCCCA TTCTTCAGAA GTTCAAGCAG 1140
GCTGACAGCA GGCTGCAGGG AAAGAGGATA ATCTACGGCT GCCCACGCTT CTCTGTGTCC 1200
CTTGGGTCCC CAGCACAGCA CTGTCCCCCA GTGCCAATAC TGGATTCTCA AAGTCTAGAA 1260
ATGAAGGCAG AAGCTGGTGT TGGAGATTTT GCCCCTTTAA TCAGCTGCAC CTCAATCCCC 1320
TCTGTGCTGG CTCAGGTTCT 1340
|
