Tag | Content |
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EnhancerAtlas ID | HS101-31950 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr4:1767170-1768750 |
Target genes | Number: 10 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BHLHE41 | MA0636.1 | chr4:1767488-1767498 | GTCACGTGAC | + | 6.02 | BHLHE41 | MA0636.1 | chr4:1767488-1767498 | GTCACGTGAC | - | 6.02 | NFKB1 | MA0105.4 | chr4:1767711-1767724 | TGGGGGATCCCCT | - | 6.04 | ZNF263 | MA0528.1 | chr4:1767587-1767608 | GAGGGAGGAGGGAGGAGGGCG | + | 6.19 | ZNF263 | MA0528.1 | chr4:1767580-1767601 | AAGGGAGGAGGGAGGAGGGAG | + | 6.32 | ZNF263 | MA0528.1 | chr4:1768224-1768245 | CGAGGAGGGAGGGGAGGGGCA | + | 6.34 | ZNF263 | MA0528.1 | chr4:1767576-1767597 | GGAGAAGGGAGGAGGGAGGAG | + | 6.41 | ZNF263 | MA0528.1 | chr4:1767583-1767604 | GGAGGAGGGAGGAGGGAGGAG | + | 7.81 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_25282 | chr4:1767656-1769984 | Colon_Crypt_3 | SE_26971 | chr4:1767576-1769093 | Esophagus | SE_33321 | chr4:1767452-1768860 | H1 | SE_34415 | chr4:1766594-1769098 | HCT-116 | SE_35570 | chr4:1767298-1769127 | HepG2 | SE_47504 | chr4:1766760-1769122 | Pancreas | SE_69102 | chr4:1767074-1769656 | H9 |
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| Number: 1 | ID | Chromosome | Start | End |
GH04I001764 | chr4 | 1766154 | 1775072 |
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Enhancer Sequence | TGCCCAGCCC ACTTCACACT GCCACCCCTG CATCCCTGGG GTCTGCTGGG TGCTTCTACC 60 TCCTCCTCCA TCCTAGCAAG CTCCTATTCA CCCCTGAAGA CCCACGCAGA GGAAGCTCCC 120 CTGACTCAGG CTAGCCTCGT CCCCTGCCCT CTGCTCAGGC TTGTCCCCTG CCCTCTGCTC 180 CTGGGAGATG GCAGTGGGCA GGCGTTCTGC AGGCAAAGCC CATGGCGGGC CTGGGTGTGG 240 ACCCCCCTCT GTCCAGGCCT CCCTAGAGGA GCAAGCCCTG CACCACCTCA GCCCTGGGCT 300 CCACCTCAGC CCTGTTGTGT CACGTGACTG CGCCCTGGAG GGATACTCAG AGGGGTGAAG 360 ATGAGCAAGG CACCTGCATT CCAGCAACGG AGCAGGCACA GAGTGGGGAG AAGGGAGGAG 420 GGAGGAGGGA GGAGGGCGTG GAGCACAGGG CACTAGTGCT GCAGCCTAGT GGGCACCAGG 480 GAGCTTTGGT TCTGACCTGG AGGTCACAGG AGCCACTGCC GGTGTGGGGT GGGGCAGGAT 540 GTGGGGGATC CCCTGGCTGC CGTGGGCACA GGGGACAGGA GGCCACCCAG GACAGCAAGG 600 TCCCTGTGGG GACTGGGGCT GGGGTCAAAC GTGAGGAGGG TGTAATTTCA GGCCTTTGTA 660 GGTGGCCTTG GGCCTAGGTG CAGGCTCACA CCTTCCCAAC CTCCTGCCCT GCCCTGGGGC 720 CCCTCCCTGA CATGGTGGGC AGAGCCCAGG CTGGCTGGGG TGCCAGGTCC CACCAGGGTA 780 TTAGGGGGCA GGGCCTGGGA GGCCAGTACC CCTGGAATCA CTCAGCTCTG GGCCTGCCAC 840 CCAGGAGATG AAAGGCCCTG CCCCTCTCAG GGCCCACATG CCCTTTGAAG GCTGTGGGAA 900 TGCCCGCAGG GCAGGCGAGT GCCAGGCGTG AGGAGGCTGC TGGGGCCATG GCGGAGGCCC 960 AGAGGATGGC CCAGGCCTGC AACGCCTCCT GCTGAGTCCC GGCAACCCTC CCAAGGCCAC 1020 ATTGTCATGC ACTTCCCAGC TCTGAGGTGC CAGTCGAGGA GGGAGGGGAG GGGCAGGGAC 1080 GTGCCCCCCC TTCTAGGCCT GGGACCCTGT CTTCCATCTG GACTGCCTGT AGAGGCAGGG 1140 GCCCTGTGGG CGGCTGCGAA AGCAGGGTTC ACCCACCCAG TTCGGGCCTT AGTGACCCGC 1200 GCTCAGCCAC AGCCACAGGG CCCTTCAGCA GGTCGCCCGA GGCCCCTCCC CCACCTCCTC 1260 TCCAGTCCAG GGTCCGAGGA CGGGTCTCCG GCCATCCCCG CCTCAGGGGT CAGCACAGAA 1320 GCTCCAGCCA GAGCCTGGTC CCTGCCCTCT TCAGACCAGG GCTGTAGGGG GATGTCCTGC 1380 CACTGGCAGG GGTCGGCCGC CTGCCCTCAC CCTCCTGGCT CCGGCGGGCG CGGCTGGAAT 1440 GTTTGCCTTT GCTGTTTGCC GGGGGAAGGG GGGGTGGGGT GAGCGCGGCC CCCCGGGGAG 1500 CCCTGTCCCG TCCAGCTGGG TCCGCGAGGC CAGTCGGCCG TGGAGGGGAC CCTCCGGCTC 1560 CGACGGGGAG TTCCAGGGCC 1580
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