| Tag | Content |
|---|
EnhancerAtlas ID | HS104-14098 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr12:53273150-53274200 |
SNPs | | Number: 1 | 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 | CTGAACTGAG AGTGAGGACA CGGAAGTTCT CACCCTGGCT CTGCCCGATG CTGCCCAACT 60
CCCCTCTCTG AGCCTCCAAA ACGACAGCGT GCTGCACCTC GGAGCCGCTG GCTCACAGGC 120
GGCTGCTTTC TCCTGGGGCC TGTCTGCTGC CGGCTTGCCT GTCCTCCTGG GTCCTGCCCA 180
CGCGCTTCTG CCCCCAGGCC CGTGCAGGCG TGGACCTCCC GCGAGGGCCT CAGCAGTCTC 240
CAGGACAGAG AGTGGAACCC GCCACCTGCT GGAAAGGCCG GAGCCGGCGC AGAGCTAGCG 300
CGGGGCAATG TGGCGCCCTC TGCGGGGAGC CCCTGCTGCC TCGCGCCGGC ACTCAAACCT 360
CCAGTACACA GTGCAGTGGA GGGCACACCA GCAGCAGCAC GCCTGTCTCA CCCTGCTCCT 420
CAGTGCCCTC CGCCCTCAGC TCCCCCCACC CACCCCCCAC CATGGCCCCT GCGTTGCCAA 480
GGGCACAGGG CATAGGAGGA CGTGGACTGA TCCACCCCAA GCTCCGCTCA CCAAGTCATG 540
CCCTAGCCTA CATTTCCCAT GAGGATGGGA GCTTCCTCTG ATTTGCACAA AGCCCCCCTG 600
TCGGTTAGTG GTGGCCTGCA ACCCAACAAC CTCCCAAGTC AGCCTCCTGG GATAGGGAGG 660
ATGTAGTGAG GGGGTGGGAG GGTGTGCAGG CTCGGCTTCC AGAAGCCGGG AGAGCAGTTT 720
CTTTCCCTGC TCCTCTGCTG CCTCCTAGTG GATGTCTGAT GTCTCTCCGG TTTGCACAAA 780
TCCATCCCGC TTCGGTCAAT CCTAGCCGTC TTGGTGCCCA TTCTTCAGAA GTTCAAGCAG 840
GCTGACAGCA GGCTGCAGGG AAAGAGGATA ATCTACGGCT GCCCACGCTT CTCTGTGTCC 900
CTTGGGTCCC CAGCACAGCA CTGTCCCCCA GTGCCAATAC TGGATTCTCA AAGTCTAGAA 960
ATGAAGGCAG AAGCTGGTGT TGGAGATTTT GCCCCTTTAA TCAGCTGCAC CTCAATCCCC 1020
TCTGTGCTGG CTCAGGTTCT TATGCTGCAG 1050
|
