| Tag | Content |
|---|
EnhancerAtlas ID | HS062-03807 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr12:53272930-53274160 |
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 | GCAGGCACAG GGGCTAAGGG TGTGAGGGGG TGCGACTTCC TCAGGGAACC CCCAGGGGAT 60
TCAGCTGCCT GAGTGGAAGG CCACGGCAGA GGTGACTTCA GCGGGGTCAG GCGGGCCTGG 120
AGTGCCAAGC TCAGGGGCTT GTGTGTCTCC AAGGAAGGGT TTGGGCCAGG CTGGGACATG 180
ATTGGGATCA ACTGGAAGGA GTGCTGTGGA GGAAGGCGCA CTGAACTGAG AGTGAGGACA 240
CGGAAGTTCT CACCCTGGCT CTGCCCGATG CTGCCCAACT CCCCTCTCTG AGCCTCCAAA 300
ACGACAGCGT GCTGCACCTC GGAGCCGCTG GCTCACAGGC GGCTGCTTTC TCCTGGGGCC 360
TGTCTGCTGC CGGCTTGCCT GTCCTCCTGG GTCCTGCCCA CGCGCTTCTG CCCCCAGGCC 420
CGTGCAGGCG TGGACCTCCC GCGAGGGCCT CAGCAGTCTC CAGGACAGAG AGTGGAACCC 480
GCCACCTGCT GGAAAGGCCG GAGCCGGCGC AGAGCTAGCG CGGGGCAATG TGGCGCCCTC 540
TGCGGGGAGC CCCTGCTGCC TCGCGCCGGC ACTCAAACCT CCAGTACACA GTGCAGTGGA 600
GGGCACACCA GCAGCAGCAC GCCTGTCTCA CCCTGCTCCT CAGTGCCCTC CGCCCTCAGC 660
TCCCCCCACC CACCCCCCAC CATGGCCCCT GCGTTGCCAA GGGCACAGGG CATAGGAGGA 720
CGTGGACTGA TCCACCCCAA GCTCCGCTCA CCAAGTCATG CCCTAGCCTA CATTTCCCAT 780
GAGGATGGGA GCTTCCTCTG ATTTGCACAA AGCCCCCCTG TCGGTTAGTG GTGGCCTGCA 840
ACCCAACAAC CTCCCAAGTC AGCCTCCTGG GATAGGGAGG ATGTAGTGAG GGGGTGGGAG 900
GGTGTGCAGG CTCGGCTTCC AGAAGCCGGG AGAGCAGTTT CTTTCCCTGC TCCTCTGCTG 960
CCTCCTAGTG GATGTCTGAT GTCTCTCCGG TTTGCACAAA TCCATCCCGC TTCGGTCAAT 1020
CCTAGCCGTC TTGGTGCCCA TTCTTCAGAA GTTCAAGCAG GCTGACAGCA GGCTGCAGGG 1080
AAAGAGGATA ATCTACGGCT GCCCACGCTT CTCTGTGTCC CTTGGGTCCC CAGCACAGCA 1140
CTGTCCCCCA GTGCCAATAC TGGATTCTCA AAGTCTAGAA ATGAAGGCAG AAGCTGGTGT 1200
TGGAGATTTT GCCCCTTTAA TCAGCTGCAC 1230
|
