| Tag | Content |
|---|
EnhancerAtlas ID | HS139-12488 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr12:53272700-53274230 |
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 | GGGGATACAG AAGCATTCCA GTCAGACTGG GCCCTGGCCA AGCTCACCGT CTGCTGGGGA 60
GGCTGTGGTG TGGTGAGAAG GGCCCTGTGG GGTAGCACAG GGTAGGGGGA GCCCAGCCTC 120
GGAGGGGCAG GGACGGCTTC CAGAGGAGGA AATCCTAACT AAATTGGGAA GATGAAAGGC 180
TCACAAGTGG ATGGGTCAGC CATAGGAGGT GCATTGCAGA CAGGGGGACA GCAGGCACAG 240
GGGCTAAGGG TGTGAGGGGG TGCGACTTCC TCAGGGAACC CCCAGGGGAT TCAGCTGCCT 300
GAGTGGAAGG CCACGGCAGA GGTGACTTCA GCGGGGTCAG GCGGGCCTGG AGTGCCAAGC 360
TCAGGGGCTT GTGTGTCTCC AAGGAAGGGT TTGGGCCAGG CTGGGACATG ATTGGGATCA 420
ACTGGAAGGA GTGCTGTGGA GGAAGGCGCA CTGAACTGAG AGTGAGGACA CGGAAGTTCT 480
CACCCTGGCT CTGCCCGATG CTGCCCAACT CCCCTCTCTG AGCCTCCAAA ACGACAGCGT 540
GCTGCACCTC GGAGCCGCTG GCTCACAGGC GGCTGCTTTC TCCTGGGGCC TGTCTGCTGC 600
CGGCTTGCCT GTCCTCCTGG GTCCTGCCCA CGCGCTTCTG CCCCCAGGCC CGTGCAGGCG 660
TGGACCTCCC GCGAGGGCCT CAGCAGTCTC CAGGACAGAG AGTGGAACCC GCCACCTGCT 720
GGAAAGGCCG GAGCCGGCGC AGAGCTAGCG CGGGGCAATG TGGCGCCCTC TGCGGGGAGC 780
CCCTGCTGCC TCGCGCCGGC ACTCAAACCT CCAGTACACA GTGCAGTGGA GGGCACACCA 840
GCAGCAGCAC GCCTGTCTCA CCCTGCTCCT CAGTGCCCTC CGCCCTCAGC TCCCCCCACC 900
CACCCCCCAC CATGGCCCCT GCGTTGCCAA GGGCACAGGG CATAGGAGGA CGTGGACTGA 960
TCCACCCCAA GCTCCGCTCA CCAAGTCATG CCCTAGCCTA CATTTCCCAT GAGGATGGGA 1020
GCTTCCTCTG ATTTGCACAA AGCCCCCCTG TCGGTTAGTG GTGGCCTGCA ACCCAACAAC 1080
CTCCCAAGTC AGCCTCCTGG GATAGGGAGG ATGTAGTGAG GGGGTGGGAG GGTGTGCAGG 1140
CTCGGCTTCC AGAAGCCGGG AGAGCAGTTT CTTTCCCTGC TCCTCTGCTG CCTCCTAGTG 1200
GATGTCTGAT GTCTCTCCGG TTTGCACAAA TCCATCCCGC TTCGGTCAAT CCTAGCCGTC 1260
TTGGTGCCCA TTCTTCAGAA GTTCAAGCAG GCTGACAGCA GGCTGCAGGG AAAGAGGATA 1320
ATCTACGGCT GCCCACGCTT CTCTGTGTCC CTTGGGTCCC CAGCACAGCA CTGTCCCCCA 1380
GTGCCAATAC TGGATTCTCA AAGTCTAGAA ATGAAGGCAG AAGCTGGTGT TGGAGATTTT 1440
GCCCCTTTAA TCAGCTGCAC CTCAATCCCC TCTGTGCTGG CTCAGGTTCT TATGCTGCAG 1500
GAATCAAGGC GAGCCTTGCC TCTCTGGCCT 1530
|
