| Tag | Content |
|---|
EnhancerAtlas ID | HS111-03914 |
Organism | Homo sapiens |
Tissue/cell | KB |
Coordinate | chr5:34656800-34658070 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF5 | MA0599.1 | chr5:34656884-34656894 | GGGGCGGGGC | - | 6.02 | | RREB1 | MA0073.1 | chr5:34657342-34657362 | TGGGGGGTGGGGGGTGGGGT | - | 6.11 | | RREB1 | MA0073.1 | chr5:34657346-34657366 | GGGTGGGGGGTGGGGTGTCG | - | 6.11 | | RREB1 | MA0073.1 | chr5:34657339-34657359 | TGGTGGGGGGTGGGGGGTGG | - | 7.47 | | ZNF263 | MA0528.1 | chr5:34657057-34657078 | GGAGGAGGTGGGGAGGGAGGT | + | 7.1 |
|
| | Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
| SE_02287 | chr5:34655256-34662593 | Astrocytes | | SE_37984 | chr5:34654574-34662301 | HUVEC | | SE_39331 | chr5:34655424-34658840 | IMR90 | | SE_45234 | chr5:34655396-34662245 | NHLF | | SE_45592 | chr5:34654572-34662834 | Osteoblasts |
|
Enhancer Sequence | GGTGGAGATG AGGGTAGAGC GGGAAGACCC GGCCAAGTTA GGAGAAGGGT TCTTCCCGGG 60
TCCTCCGCGA CTCGCAGGCC GGCTGGGGCG GGGCGCGGGG CAGGGGCCGC GGCGGAGGGA 120
GCGCGGGTGG GAATGAATGA GCAGACCCGG AGATGCACCC TGGAGTCTGC GCCGGGTCCC 180
ACCTGTTTCG CCCCGCGCGG CGCCTCGCTG CCCCCGCGTC GGTGCTGCTG AGCCCAATCC 240
GCCTCCCGGC TGAACTTGGA GGAGGTGGGG AGGGAGGTGC GAGCGGGAGA CTCCGGGTGG 300
CTCCCAGGAC GCGGGGTCCG CTATTGTTCC TCCTCTGACT CCAGGGAGCC CCTCGGCCGG 360
CCCAAGGGCG GGGGCGAGAC CCCTCTGGGC CTGCCCCTGC CCCCTACCTT GTTTTCCCCG 420
CCGCAGCTCG GGGAGAACGG ATGCTGGAGT TGGGGCAGAC TCGGGGCCGC CGGGACTTCG 480
GGAGTAAGGA GGACGTGGAG CCACCAGAAA GGCGCCCGCC ATCTCCCGCG ACCCCTGCCT 540
GGTGGGGGGT GGGGGGTGGG GTGTCGTCCT CAACCACCTT CGCTGCCTTC TTGGGCAGGT 600
TGGTGTCGGT TTAGTTTCTG CGGTTTGCAG GGTTGACATC CTAACTCCTT TGAGTTTCGC 660
ATCCCCCTTT TGTGGAGGGG GCTCAGAGCC TGGAGAAGCA ACAGACGGGG AATTAAGGCA 720
GATGCAGCCC AGCACAGCGT GGAGGGGTCC GAAGTGGCCT CACGGGGGCC TGAGCATGGC 780
TGTCTTTCCA GGCTCCTCTT TATTTGCCAG GAGCCCAGCT AAGCCCAACT TTACTCCCAG 840
AAATGTTGAG GGGAATCTGC GGACTCGAGG CCCCTCGCCT CGGGACCAGC GGCTTCTCTT 900
CGCCGCAGCT CACGCATGAT CGGGGTGGGA TTCCGTCTTC CTTCCGGGAG AGGAGAATGC 960
CCAGCTGCCT GGGATGGGGA AACGTTGCCG GATCTCTGGG GAATGTGGTC TCAAGGCTGC 1020
AGGGGCCTGG CAGAGAGGAA CTGTCCATCA CTAGGACATA GCCGAAGCTC GCCTTAGCGA 1080
AGAGAGTCTC ACCTCCTCGG GCTTTGCACA GAGTTGGAGA AGAGGTCGGG AATCACAGGG 1140
AGGCTGGATT TTGGCTGCTC TGTCCCCAGC CTGCAGGTCC CTGTTCGCCC TGTGGCTCGG 1200
AATTTTATTA CTGATGTATA TAATCTGATA ATCTTTTCTT AATGATGCCT AACAAGTGTG 1260
ATTTTTTTCC 1270
|
