Tag | Content |
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EnhancerAtlas ID | HS047-07966 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr12:53272840-53274160 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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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 |
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| 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 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I052878 | chr12 | 53272285 | 53274184 |
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Enhancer Sequence | CAGAGGAGGA AATCCTAACT AAATTGGGAA GATGAAAGGC TCACAAGTGG ATGGGTCAGC 60 CATAGGAGGT GCATTGCAGA CAGGGGGACA GCAGGCACAG GGGCTAAGGG TGTGAGGGGG 120 TGCGACTTCC TCAGGGAACC CCCAGGGGAT TCAGCTGCCT GAGTGGAAGG CCACGGCAGA 180 GGTGACTTCA GCGGGGTCAG GCGGGCCTGG AGTGCCAAGC TCAGGGGCTT GTGTGTCTCC 240 AAGGAAGGGT TTGGGCCAGG CTGGGACATG ATTGGGATCA ACTGGAAGGA GTGCTGTGGA 300 GGAAGGCGCA CTGAACTGAG AGTGAGGACA CGGAAGTTCT CACCCTGGCT CTGCCCGATG 360 CTGCCCAACT CCCCTCTCTG AGCCTCCAAA ACGACAGCGT GCTGCACCTC GGAGCCGCTG 420 GCTCACAGGC GGCTGCTTTC TCCTGGGGCC TGTCTGCTGC CGGCTTGCCT GTCCTCCTGG 480 GTCCTGCCCA CGCGCTTCTG CCCCCAGGCC CGTGCAGGCG TGGACCTCCC GCGAGGGCCT 540 CAGCAGTCTC CAGGACAGAG AGTGGAACCC GCCACCTGCT GGAAAGGCCG GAGCCGGCGC 600 AGAGCTAGCG CGGGGCAATG TGGCGCCCTC TGCGGGGAGC CCCTGCTGCC TCGCGCCGGC 660 ACTCAAACCT CCAGTACACA GTGCAGTGGA GGGCACACCA GCAGCAGCAC GCCTGTCTCA 720 CCCTGCTCCT CAGTGCCCTC CGCCCTCAGC TCCCCCCACC CACCCCCCAC CATGGCCCCT 780 GCGTTGCCAA GGGCACAGGG CATAGGAGGA CGTGGACTGA TCCACCCCAA GCTCCGCTCA 840 CCAAGTCATG CCCTAGCCTA CATTTCCCAT GAGGATGGGA GCTTCCTCTG ATTTGCACAA 900 AGCCCCCCTG TCGGTTAGTG GTGGCCTGCA ACCCAACAAC CTCCCAAGTC AGCCTCCTGG 960 GATAGGGAGG ATGTAGTGAG GGGGTGGGAG GGTGTGCAGG CTCGGCTTCC AGAAGCCGGG 1020 AGAGCAGTTT CTTTCCCTGC TCCTCTGCTG CCTCCTAGTG GATGTCTGAT GTCTCTCCGG 1080 TTTGCACAAA TCCATCCCGC TTCGGTCAAT CCTAGCCGTC TTGGTGCCCA TTCTTCAGAA 1140 GTTCAAGCAG GCTGACAGCA GGCTGCAGGG AAAGAGGATA ATCTACGGCT GCCCACGCTT 1200 CTCTGTGTCC CTTGGGTCCC CAGCACAGCA CTGTCCCCCA GTGCCAATAC TGGATTCTCA 1260 AAGTCTAGAA ATGAAGGCAG AAGCTGGTGT TGGAGATTTT GCCCCTTTAA TCAGCTGCAC 1320
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