Tag | Content |
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EnhancerAtlas ID | HS047-15935 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr18:45591140-45592580 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NRF1 | MA0506.1 | chr18:45591512-45591523 | GCGCATGCGCA | + | 6.32 | ZNF263 | MA0528.1 | chr18:45592323-45592344 | GCTCACCCCTCCTCCTCCTTC | - | 6.42 | ZNF263 | MA0528.1 | chr18:45592317-45592338 | CTCTCTGCTCACCCCTCCTCC | - | 6.49 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_26544 | chr18:45590308-45593361 | Esophagus |
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| Number: 1 | ID | Chromosome | Start | End |
GH18I048063 | chr18 | 45590309 | 45593361 |
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Enhancer Sequence | GAACAGGGAG AAGAAGGTGG TCCCAAGGCA GGGCCCCCCG GGAGGAGTAG GATGCAGGCT 60 GAAGTGGACC CTAGAAGTTC TGCTCTAGAG GAAAATGGCA GGAGAAGACC TGGAACAAAG 120 CAACAAAGCC CACAGAGGGC TTCTCGAAAC ACCACCTCCC TCCTTCAGGG TACTCCTAAG 180 CTCCCACCAC TCCACTCAAG GAAAGGACTC TGCAGTCACA GACTTTAACC GCCAAACATC 240 TAACATGTCC TTTTGGTTGG GAGAGGCCCT GTGGGGAGAG TTTTGATGGT AGGAAGCAGG 300 ACTCTGCCTC CCACTGAGGA AGAGGGGCCT CCTTCCACTC CCAGTGCCCC CCGCCCCCTC 360 CCTGTCCAGC GAGCGCATGC GCACACAGCG CTAGGCCCAG CTGGCTGGAC CCCGCTGCCA 420 GGACCTTGAA TCTTAAGTGA GTGACAGTTA GCAGCAGCAG TTTGTGTTGC TTATTTGCAA 480 CTATGAACTT TGAGTGACAT AAATGTTGGG CATACCTGAA TACCAGAGCC TTGCTGGAGA 540 TTCGCAATGA ATCTCTCTCT CTCTCTCACA CACACACACA CACACAAACA CACACGCCTG 600 AGAAAGCCCA TAGTATAGAA ACCTGTTTAA CTTTGTTTAA CTCTGCATTT CCCAAACTTG 660 TTTAATCTTT CTGCTTTGCC TAACGCCTTT TAATATCCTG CAGAACTGGT GTGACAAGCA 720 CACCTTCAGG TAACACTGGG GGTAGAGCCA TGCTTTCCAA ACTTTTTCAG TCATGGAATT 780 TGCAGAGAAA CACTATTTTT ATGGCACAAA GGAATTGGAG GGCTCTCAGG AGGTTGCTGG 840 GCTGTTCAGC TGACAAGAGG CATGAAGGGG CAAAGCCACT GGTTGGGAAG CTGTGGACCA 900 GAGGACAGAG CCCTCTGGGA TACAAGCCTG GAGGCCTGAC CTCTCGCCCT GGCTCTGGTG 960 TGAAGCAGCC TCCATGAGGT CACACAGGTA GCTGCGGCAT CCCAGGGCCT CCTCTACTGT 1020 ACCATACAGT TTCCCTCTAG GGCCGTTGGA GAAGTGGTCT TATCAGAGGA TGCCTGCTTT 1080 CTCTGAACAG AAATGAGGGG GCAGAGTGGG GCAGCTCATC TTCCAATACA CCCCCATCCC 1140 TGGAATTAGC TCAGGGTCAG GACTTGCCAG CTCTGCCCTC TCTGCTCACC CCTCCTCCTC 1200 CTTCCCAATA AGTTCTGGAT CCAGCCCTAG TAGGCAATGC ATGGAAGCTT CTTGTGTGAG 1260 GAAGCCCACC CATTTGGAGG TCTTCTGTCT CTGCATGTGG TATCTGCTCT CTCCTTCATC 1320 TGCCAGCCAG GCATCATCTC CTAACCTTCG GCTTCCATGC TGTTCATCTC CTGAGGCCCC 1380 ATAATCCTTG CTGGCATCCC TGGGGACTGG GCTAGTGCCC ACCCTGGCTC CACCAGCCTT 1440
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