Tag | Content |
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EnhancerAtlas ID | HS091-00357 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr1:9926340-9929080 |
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) |
CTCF | MA0139.1 | chr1:9927706-9927725 | CAGCGCCACCTAGTGGGCA | - | 7.54 | PLAG1 | MA0163.1 | chr1:9927319-9927333 | GGGGGCCACTGGGG | + | 6.13 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_26899 | chr1:9928755-9933850 | Esophagus | SE_60796 | chr1:9907685-9935747 | DHL6 |
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| Number: 2 | ID | Chromosome | Start | End |
GH01I009867 | chr1 | 9927381 | 9927530 | GH01I009868 | chr1 | 9927621 | 9927830 |
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Enhancer Sequence | AAGGCATGAA CATGGCCATT CACTATGGCC CTTTACAGTG TGAGGTCAGG TCTTGCTCAC 60 CAAGCTAAAG GGGCTGGATT TTATCCTCAA GGCAGTGGGG AGCCACTGAA TGATTTTAAG 120 TTGGGTGGAG GCTGGGCATG GTGGCTCCCG CCTGTAATCC CAGCACTTTG GGAGGCCAAG 180 GTGTATGGAT CACCTGAAGT CAGGAGTTTG AGACCAGCCC GGGCAACATG GTGAAACCCC 240 GTCTCTAATC AGCTGGGTGT GGTGGCGGGA GCCTGTAACC CCAGCTACTC GGGAGGCTGA 300 GGCAGGAGAA TTGCTTGAAC TGGGAAGGTG GGGGCTGCAG TGAGCCGAGA TCACGCCACT 360 GCACTCCAGC CTGGGTGACA GAACAAAACT CCTTCTCAAA AAAAAAAAAA AAAGTCGAGT 420 AGAGACCCAC TAATGTCACT CTAAGCCTCC AAAAGTCTCT CCAGCTGTGG GGGTAGAGAG 480 CAGACCTGAG GGGGCAAGAT GGGAAGTCGA GATGCCAGAT AGGAGTGATC TGAAGCTGTG 540 AGACAAGAGT GAATATGGGC TCAGTCCAAG AGGGGGCTGG AAATGAGAGG GAGAGAATGA 600 AGCAGGTCTG GGGAGCCTTA GGATGGACTC AGTAACCCAT TAGGTTCCTG AGGAAGAGAG 660 GAGTCGAGGC TGAGTCCTCG GGCGCCGTGT ACTTGCTGGG CATTGGTCAG GGCAGAGCAC 720 AGGTGGAAAA TCCATGTCAG CTGGGCATGG GTGGCTGTGG TGATGCTGGC CAACAGTCAG 780 CTGGCTATGT TCTCTGTTGA GATCACAGCA CTGCGTGTGG AACAGGGAGA AGAGAGGGGG 840 CAACCCTGGA GGATGACAGC CCTGATTGAG GGAAGGGAGT GGGAAACAGC CAGTGAGGGG 900 TGACGTGAAG GACAAGGGAG GGAAAGGAGG CTGTCATTGG TGGTCTCAGC CCAGCAGAGG 960 CCAGGCAGGC TGGGAACTGG GGGGCCACTG GGGCCTCTGC TGGAACCACC TGGTGAGCCC 1020 GTAAGGGGAG GCCCCCACCC CAGGGTCTCC AGCACCTGCC TGGCTCCCCA TAGATACTCA 1080 ACAAATGTGA CCGAGGAAGG AATCGAAGGG TAGGGGGTAA AGGGGTGCCC ACGGCCCCCT 1140 CCCTGGGCCT CAAGTAAGGG AGCAGTGCCC CAGGTACCAG ACCCATCCAG CCCTGGAGGG 1200 GAAGCATGTG CAGGGCTAAA GGTGGCGGCC AGACCCTCAG GACCAAGGTC GGGTGCTGTC 1260 CGTTGGAGGG TCTGCCTCAG ACCCCCTGCT AGAGGAGTCC CGGGGTAGAT GGAGCCTCCT 1320 CTGGCTCAGG GAACACCTAA AGCAGCCTGG AGCATTTGCT GAGAGACAGC GCCACCTAGT 1380 GGGCAGGAGG TGCACGCCAG GCCATTACCC ACAGGCTCCA GGCCTTTGGG GTTCATTATG 1440 GCAGTCTCTG CACCCTGCTC TGGCCCCCGC ATCCTGCCCC AGTCCCTGGA GACAACAATC 1500 CAGGGCTTCT TCCACCTAAG CAGTGTCTGA GCCTCTGACA GCAGGATCCT GCAGCATCAG 1560 CTGAGATTGG CTCTGCGATG GAGAAGGTGG GCAGGTGAGA TTTTAACAGA GATCCATTTG 1620 CCCACATGGC ACAGGCAGAT GCAGGGTCCT GCCCTCACAT GGGTAAGCCC AGTATGGGAC 1680 TGGGCTGATT GCAGTTCTGC TGTTATTGTT GTTGTGTTTG TTTGTGGTGT CGTTAGGCTC 1740 GCAAAGAAAA TAAATATGCT TATGAAACTC TTCCAGACAT GGCTGACCCC TCCCCTCTCC 1800 ACTCCCAGTC CACAGAATTC TCAGAACCTC CTGCAGCTCA GGTCTGTGTG GCTCAGGCCC 1860 CGGCAGCCAG GTTAGAGGTA TCTTTATGGA GGTAGGGGCA GTCCACAGGG CGCCCCAGCA 1920 GCAGGGAGTG ACTCCCACCA CCTATTCCGC AACGATTCCC TGGGGTCTTC CCTGGCTCCA 1980 GCTTCAGCTC CAGAAGACCC CTCCCCGGAG AAAGAAGTAG CTGTGGACAG ACACCACCCA 2040 CCCAGAAGGG CCTGGACTCC ACGGCCCACA CAGTTGGTCA CAGCTGCCAG CTTGCTCCTA 2100 CTGCTCAGCA GTTTCAGGGC AAGGTCAACA GCTAAGTGGG GTCACTGACC TTCCTCAACA 2160 ACTTGGCAGA GCTCATTTTT ATTCTTAACT GTGGGTTCGG CTAGGCAAGA GTTCTCCTAA 2220 AAATATTTTT TTTAACTTTC CCTTATGACA AAGAAACAAA TGTACAATGT TAAAATATTA 2280 GTTTTACAAA AATGTGTGAC TTGGAAAGTT AAAGTTTCTT ATATAGTCCT ATCCCCTAAC 2340 AATTATTATT ATTATTATTT TTTGAGACAG AGTCTAGCTC TGTTGCCCAG GCTGGAGTAA 2400 AGTGGTGTGA TCTTGGCTCA TCGCAAGCTC CGCCTCCCAG ATTCAAGCGG TTCTCCTGCC 2460 TTAATCTCCC AAGTAGCTGG GTAGCTGGGA CTACTGGCAC CTGCCACCAT GCTCAGCTAA 2520 TTTTTGTATT TTTAATAGAG ACAGGATGTT GCCATGTTGG CCAGGCTGGT CTTGAACTCC 2580 TGGCCTCAGG TGATCTGCCC ACCTTGGCCT CCCAAAGTGC TGGGATTACA GGCATGAACC 2640 ACCACGCCCA GCACCCCTTG TCAAAAACAA AATTTCTGAC AGTCTGGTAT ATATTCCACC 2700 AGCTTCTTTG TCTTTTAAAA ATTTTTTAAA TTTATGAGAC 2740
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