Tag | Content |
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EnhancerAtlas ID | HS104-46791 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr5:35802820-35803960 |
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) |
RFX1 | MA0509.2 | chr5:35803371-35803387 | TGTTGCCATAGCAACA | + | 7.1 | RFX1 | MA0509.2 | chr5:35803371-35803387 | TGTTGCCATAGCAACA | - | 7.1 | RFX2 | MA0600.2 | chr5:35803371-35803387 | TGTTGCCATAGCAACA | + | 7.37 | RFX2 | MA0600.2 | chr5:35803371-35803387 | TGTTGCCATAGCAACA | - | 7.4 | RFX5 | MA0510.2 | chr5:35803371-35803387 | TGTTGCCATAGCAACA | + | 7.57 | RFX5 | MA0510.2 | chr5:35803371-35803387 | TGTTGCCATAGCAACA | - | 7.58 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_11984 | chr5:35802748-35804165 | CD3 | SE_14792 | chr5:35802600-35804219 | CD4_Memory_Primary_7pool | SE_17815 | chr5:35802437-35804983 | CD4p_CD25-_CD45ROp_Memory | SE_18247 | chr5:35802549-35805999 | CD4p_CD25-_Il17-_PMAstim_Th | SE_62940 | chr5:35777138-35837406 | Tonsil |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I035802 | chr5 | 35802881 | 35803702 |
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Enhancer Sequence | AACTGGTGTG CTCTGAGAAC TAGGGCTAGC CAGCAGAGCT GGAGAGGACC AGGCTGAAGG 60 AGAGTAACAG GGAAGGGAAG TGAGAGGGAG AGGACCCTGA GGTCCACTGC AGGGACCTTA 120 GCTTTAACTC TATGCAGGAT GAGAAGTCAT TGGAAGGGTG CAGTCACCTG GCTTCACTAA 180 GTCAGGATCT CTCTGTGTTG AGGAGAGACT ACAGACGGCA AAGGAGGGAA GTAAGGAGAC 240 CTAGGCCTTC AGGCAGGGGA CCACTTATCT ATTTCTACTG CTAAATGGTT CCTGCCTTGA 300 GTTTGGGACA CCTTGTTACC CATCTTCATG TCCTCTGAAG TAGCTGCCAC ATAGCCAGTG 360 CTTGATTAGT ATTTGTGAAC ATGGCCAGGA AAGAAGTGAA GAAGGAAGAG AGGGACAGTG 420 AAATGAATGG AGTTTAGTCT CCATGGTAGA GAGGAGGAAA GCAGACATTG CAGGCAGGCA 480 GAGGCAACAG CGGAGTCCAG GAGGCTGAGA TGAGCAGGAA AGGCCAGGAA AAAGGAAGCC 540 TGTGCTAGAG CTGTTGCCAT AGCAACAGAC AGCTGTCTCC TGAGGCTGGC AGCCAGGCTA 600 GCTAGCACAG GAAGACGCTT AATGCCTTCC ATCCCTGAGT GCTGCATTCA CTGTGTGCTA 660 GTGTTCCTAC CCGGGAAGCA GCTCTCCTTG AGTGCTGCTC TCAAGAGCTC CTTTAAAATC 720 CAAGGACACT GTGGAGGAAC TGAACCAAGA ACACTGCGCT GCAGAGATTA AGCTAGTGGG 780 TGGGAGGTGG AGCCTGGGAT GGAACACAGG GCTCTCTCTC ACACACAGGC CTGTTCCTGA 840 CTTGGAGTGA ACCCTAGGAG CACTTGGAAC ACAGAAGCCA CTCACCTTCT TCATTCTCAC 900 TCACTCCTCA TCCCACTGTC TCCAACTGTG GCACTCCATT TCTGTGCCAT TTCCACTGTG 960 TTCCAGTTTC CTGGGCAACC CTGTCCCAGG AAGCCATAAT GCTCAGAAAT AACACCTCTA 1020 GCAGATTCAT ATTCACTCCC AAGCCATTCA ATCAGATCTC TGCTTTTGCT TTCCCCACAA 1080 ACAACTGGAA ATCTCCCCAG CATTTCATTC TTCTTTACTC TATTTCTGCT ATTCATGCTG 1140
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