Tag | Content |
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EnhancerAtlas ID | HS182-21637 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr9:91391320-91393680 |
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) |
RREB1 | MA0073.1 | chr9:91393147-91393167 | TGGGTGGTGGTGGTGGGGTG | - | 6.82 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_36802 | chr9:91389349-91392745 | HMEC | SE_38646 | chr9:91388475-91394098 | HUVEC | SE_56572 | chr9:91385647-91393268 | u87 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I088773 | chr9 | 91388661 | 91393535 |
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Enhancer Sequence | ATTTTTCTCT TCTGGAGAGC CAAGAGCCTG AAAGGTAGAA TTGAGAGCCT AGAGAATCGA 60 GCCCACGACA CAGTGAGGAT AATTCCTTAA ACTTAATTGC ATCTCCCAGA TGGATTGAAA 120 CTGCCTGAAC TGGTGCCCCC CATTTTCCCC TTTTGGAACC AGAATGTCTA TAATGGCTCT 180 CCTACACTTA TACCATCATT GAATTTGGTG GTCAGATTAC TTGTTTTCTA GTTTTACAGG 240 GCCACAGATA GACAGGGTCT GTGGCTCAGG GTGTATCATA GCAGAGCCTC ACCTGACTGC 300 TCAAGGCGAC TGAAATGATG AGATTTTGGA CTTGAAGTGG GTGTTCTAAT GGAGTGAGAT 360 CTTTGTTGTC ATGAGACAGG ATAGATGCAT TTTGCAGATG AGAGAGAGGA ATGTGGTCAG 420 AGGGTAAACT ATAGCAGACA AAATTTTTGC CTCCCCCATT TTAGACCTGC CTTTTAATGG 480 ACTTGCTTAG TCATTGGGGT TAACTATGAG CAAACACAGT CCCCAGTACA GCAGAACAGA 540 GAAACAACAA TGTACCAGGT TAGATCAGAG CAAAGGAATG TTTGAAAACT GGAAACATCT 600 CATATTTAGA AAACAAGAAG TGGGCAAGAA ACCAGAGTGT CTGGGGAGCC TATAAGTGCA 660 TATGAAAAAG TATGGGCCCA CGTTGGGCAT GGTGGCGCAT GCCTATAATC CCAGGAGGCT 720 GAGGTGGGAG ATCGGGTGAA TCCAGGATTT CAAGGCTTAA GTGAGCTCTG ATTGTGCCAC 780 TGCACTCCAG CCTGGATGAC AGAGTGAGAC CCTGCCTCAA AAAAAAAAAA AAATAAAGGC 840 ACAAATGGAA GGTGTTTGTA TCAACAGGGC CAGGGCCATG GGCTCTTGGA GTGCCAAGTG 900 TCTCAGACGC AGCATCAATC GTCAGCAGTA GTTGTGGTTC CTCCTTCTGC GTGGTCACCT 960 GTGGAGGGCC TGCAGTGAGT GTGCATGTGT GTGTGTGCAT GTGTACGGGG CATAACACTG 1020 GTGGCAAAAC ATCAGGGAAA ATCTGGGGCT TCTGTGTTCA AGAAATTAGT TTTATTGTAA 1080 TTGTACAGAG ATAAAATCCC TACTTTCACA GAGTATTCTT ACGCACTACT TTCTTTTCTT 1140 GGAAATTTTG GGGGGAAAGA CTAACAATAC ATGTTTCTTA GCCGTGGCCT TTCCTAATTT 1200 CCAAGAGCTG AATCTCATCC TGCTAAGGTC TCCCTGAAAC CAGACTGCTC TGCACCCTCC 1260 TCCGCACTCC TCCCCACGGC ATGACAGTTA CTGCCCATCT TCTGAGATAA CTTCAAGGCA 1320 ACTATGGCAG CTTGTTTTAT TTTCTCTTCC TGCAACTCTC TCTGATTCTC TCTTTCAGCA 1380 TTTAAGGATT GTCTTACTCT AATCAGCAAC TCCACCAGGA ACCTTTTGTG TTTTTTCGCT 1440 CTGTTTCTCC CCCACTATTT GGGGCCAGAG CCCTCTGAGC CTCACATAAT GAAATTCAGG 1500 TCGCTGTGCA GAAAATATTG AGCACAGAGA AACAAACCCC AGGAGGCAAA CTCTGAGGCC 1560 GGAAGGTAGA ATTAGGAGCA GCCAAAAAGG ACAGCAGGCG AGTTCAACCG GATGCATGAT 1620 CATTTCCTGT TCTTAAAATT CCCTTTAATA TCCCCAGCCC AGCCCGCTGA GTCGGTGAGA 1680 AGCTGGGGAG GAAGAGCCCT GGCTGGGGTC AGGGGCCCAG GCTGCAGGCC CAGCTGGTGG 1740 CTCGCTAGTG AGGCCCTGGG GAGACCTCTC AGGCCTGTCT TCAAGTCAGT AAGGAGGGGC 1800 CAGTCCTGCA GCTCTACCCT CAGAGCATGG GTGGTGGTGG TGGGGTGTGT GTGTGTGTGT 1860 AAGGCAGGTC TGGCTCCAAG CATCAGGAAG TGAGAACTGG GGAGAGATGT CTTTTGTGGG 1920 GTTCACACCC TCCCCAGCCG GGTTCTCCCA CTCTCCTGGA AGGAACGGGC AGCTAACACC 1980 TCAGAGCTCC TGGAACAGGC AGGGGATGCC CACCTCCTTA TCTCAGGGAG TAACCTGTGC 2040 ACAGTCCTGG GAACAGGCAC GGTCATCTTA GTGATAGTGA CAGTGTGGCC TGGCCTGCAG 2100 CAGTGAGTTC TGCACACTTC ATTGCGGGGA AGCTGGATGG TAGAAAGTGG AGACATTCAA 2160 CCAAGATGAC GCAGTTGTTT GCAGCCACAT GTAGAATTGA CGCCTGTCTG AAAACCTCCC 2220 CACCATTTGG CCACGATCAG TGCTGACCCT CACTCTGTCC CTGGGCTGTG GCTGACACAC 2280 ACAGGGTCAC TGCCAATTGC TCAGGGCTCC TGTCTCTCAA TACATGTATT TTCACAAAAA 2340 GGACACTCAC TAAAGTGATG 2360
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