Tag | Content |
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EnhancerAtlas ID | HS111-02596 |
Organism | Homo sapiens |
Tissue/cell | KB |
Coordinate | chr19:14528960-14530080 |
Target genes | |
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) |
KLF16 | MA0741.1 | chr19:14529954-14529965 | GCCCCGCCCCC | + | 6.02 | KLF5 | MA0599.1 | chr19:14529954-14529964 | GCCCCGCCCC | + | 6.02 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_09406 | chr19:14526541-14531363 | CD14 | SE_18377 | chr19:14526473-14531096 | CD4p_CD25-_Il17-_PMAstim_Th |
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Enhancer Sequence | AGAGAGAGAT AAATAAATTG GGGTGAACCG AATCTGCTAA GATAAAATTT TCGAGAAACC 60 GGGCTGGACA GGATCTAAAG CTCAAAACTG ATTAGATCAG GAAAGGATCC GGCGGGGTTT 120 TCCCCGCCCA AAGTGGGTGG CCATGACCGC TAAGGCGCCA GGAGCGCATG AACTTGAAAG 180 GTGACAGCGG GGAACTCACA ACCCAGACAC GCCACGTGTA CCCAGTTACC CTCAAGTGTC 240 CCCAGGCAGG CTTTCCACCC CGGAGTTTAT TCCCACCTGG GGACTCCTAT TTCCAAAAGA 300 AAATCTTTTT TTCATTCTGT TTTTTTTGAG GCAGAATCTC GCTCTGTCAC CCAGGCTGGA 360 GTGCAGTGTC GCGATCTCGG CTCACTGTAA CCTCCACCTC CCGGGTTCAA GCGATTCTCG 420 TGCCTCAGCC TCCCGAGTAG CTGGGACCAC AGGCGCTCGC CACCACGCTC GGCTGATTTT 480 TTTTTGTATT TTGAGTAGAG ACGAGGTTTC ACCATGTTGG CCAGGCTGGT CTCGAACTCC 540 TGACCTCAAG TGATCCGCCC TCCTTGGTCT CTCCCAAAGT ACTGAGATTA CAAGAGCCAC 600 CGCGCCCGGC CTTCCAAAAT AAAGTCTTAT TTGCTCTAAA TCTCAGAATC CCGAATCCCG 660 TAAAAAGTAG ACCAAGAAGA AGGTAGACTG GGAAAGGGAT CAAGTCCCTC GGACCCAAAG 720 AAACCCCTGA CAACTGAAAG CTCCAACTTC TCCCACCCAG GCCCCAGACC CCGGCGTCAC 780 CCCCTCGTCC CTCTCCAAAT GGCCCCAGGC CGCCGCGGGG TCTATTCGGA CGAACTGACA 840 GACTCCAAGT GGGGCTCGGA GCGCCGTAGG CCATGACAGC CCCTCCGAGA AGCGGGCCCC 900 GAGCCCCGAG CACCGCGCGC CAACGGCTGG CCCACCCCTA GCGCATGCGC CCCGGTGCCC 960 AACGGCCAAC ACACAGCGCT CTGACACACC AACCGCCCCG CCCCCACCGT CTCGCGACCC 1020 TTTCTCCCCC TCCCCTTAGA TCCCAACGTC TCCCCTCGTC CTCTCGCTCT CAGTTCAGAC 1080 GTCCCCACAC CGCGGCCCCG CGCCCGGGAT CCGCTGCTCA 1120
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